Senior Technical Product Manager jobs at Johnson & Johnson - 694 jobs
Sr. Product Manager, Peripheral Portfolio Strategy- Shockwave Medical
J&J Family of Companies 4.7
Senior technical product manager job at Johnson & Johnson
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************
**Job Function:**
Marketing
**Job Sub** **Function:**
Strategic Marketing
**Job Category:**
Professional
**All Job Posting Locations:**
Santa Clara, California, United States of America
**Job Description:**
Johnson & Johnson is hiring for a Sr. ProductManager- Peripheral Portfolio Strategy - Shockwave Medical to join our team. This role is fully remote with 60% travel.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************/ .
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Ready to join a team that's pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
**Position Overview**
We are looking for a high-performing individual to join our peripheral portfolio strategy team to lead new peripheral development projects. This individual will work with peripheral team members to guide the direction of programs by engaging with Key Opinion Leaders (KOLs); exploring unmet needs and market opportunities; and collaborating with R&D, quality, regulatory, marketing, sales training, clinical, operations, manufacturing, and sales teams. The ideal candidate desires to be part of a fast-paced, collaborative and innovative team backed by one of the most exciting companies in medical device history. This is a visible role that will be vital to the company's success.
**Responsibilities:**
+ **Product Strategy Development** : Lead the development of upstream product strategies by analyzing market trends, customer insights, and competitive landscapes to identify growth opportunities and unmet needs.
+ **Clinical Insights and Engagement:** Attend cases to observe procedural workflows, understand technology adoption and gain insight into clinical decision making and utilization patterns to inform product strategy and development.
+ **Cross-Functional Collaboration** : Collaborate with engineering, design, sales, and marketing teams to ensure successful product development, positioning, and launch. Provide clear product requirements and business case support.
+ **Partner with Development Team to Evaluate New Products** : Collaborate closely with the product development team to assess new products through hands on preclinical evaluations in animal and cadaver labs.
+ **Market Research & Analysis** : Conduct in-depth market research and competitive analysis to inform product positioning and identify new features or enhancements that address customer pain points.
+ **Customer & Stakeholder Engagement** : Engage with key stakeholders, including customers, internal teams, and leadership, to validate product concepts, gather feedback, and ensure alignment with customer needs and business objectives.
+ **Product Lifecycle Management** : Take a leadership role on project teams and work closely with the project manager to drive accountability and team achievement of goals and milestones.
+ **Metrics & Reporting** : Define key performance indicators (KPIs) to measure product success and continuously monitor and report on product performance against objectives.
**Requirements:**
+ Bachelor's degree in Business, Marketing, Engineering, or a related field. MBA preferred.
+ Minimum of 6 years of related experience required. Experience in medical device, vascular devices preferred, and catheter experience ideal.
+ Proven experience to become a subject matter expert for a variety of new clinical applications, community trends and more specifically, the segments targeted by assigned products.
+ Ability to develop relationships with key opinion leaders and to modify strategies and tactics when necessary, based on voice of customer and emerging trends.
+ Attend clinical cases to uncover unmet needs, observe workflow and better assess and understand new disease states and procedures.
+ Excellent collaboration and communication skills with ability to influence, gain the respect/buy-in from stakeholders and all levels of management across Shockwave Medical.
+ Cross-functional team leadership experience preferred.
+ Ability to collaborate and work with others in a dynamic, matrix environment.
+ Ability to work in a fast-paced environment as individual contributor or as part of team, while managing multiple priorities and adapting to changing requirements.
+ Ideal candidate will be local to Santa Clara office, remote candidates will be considered with expectation of monthly travel to Santa Clara office.
+ Must be able to travel up to 50% for local candidates, up to 60% for remote candidates (Global & U.S.).
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via *******************/contact-us/careers or contact AskGS to be directed to your accommodation resource.
**Required Skills:**
**Preferred Skills:**
Brand Marketing, Brand Positioning Strategy, Business Alignment, Business Storytelling, Business Valuations, Cross-Functional Collaboration, Customer Intelligence, Data Analysis, Data-Driven Decision Making, Digital Strategy, Execution Focus, Financial Analysis, Go-to-Market Strategies, Industry Analysis, Market Research, Negotiation, Problem Solving, Process Improvements, Product Development Lifecycle, Product Improvements, Product Portfolio Management, Product Strategies, Strategic Thinking, Tactical Planning, Technical Credibility
**The anticipated base pay range for this position is :**
$118,000.00 - $203,550.00
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
For additional general information on Company benefits, please go to: - *********************************************
This position is eligible to participate in the Company's long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
$118k-203.6k yearly 3d ago
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Sr Product Manager, Copy Review and Digital Asset Management
Johnson & Johnson 4.7
Senior technical product manager job at Johnson & Johnson
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************
Job Function:
Technology Product & Platform Management
Job Sub Function:
TechnicalProductManagement
Job Category:
People Leader
All Job Posting Locations:
Athens, Georgia, United States of America, Cincinnati, Ohio, United States of America, Danvers, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, Irvine, California, United States of America, Jacksonville, Florida, United States of America, Malvern, Pennsylvania, United States of America, Mooresville, Indiana, United States of America, New Brunswick, New Jersey, United States of America, New York (Any City), Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, Santa Clara, California, United States of America, Spring House, Pennsylvania, United States of America, Tampa, Florida, United States of America, Titusville, New Jersey, United States of America, Warsaw, Indiana, United States of America
Job Description:
Johnson & Johnson is recruiting for a Senior Technology ProductManager, Copy Approval and Digital Asset Management. The preferred location for this hybrid role is Raritan, NJ, United States. Other J&J locations in the US will be considered on a case by case basis.
Come join our exceptional team at Johnson & Johnson as a Senior Technology ProductManager, Copy Review and Digital Asset Management! This role offers you the chance to make a significant impact on our digital asset management and copy review process. We are looking for a highly motivated individual who is passionate about technology and has a proven track record of successfully implementing digital solutions. If you are driven, have a passion for excellence, and enjoy working in a collaborative environment, this could be the ideal position for you!
Key Responsibilities:
* Lead the technical end-to-end development lifecycle of our software product, from planning to deployment.
* Act as a technical advisor to seniormanagement, providing insights and recommendations on technology trends, risks, and opportunities.
* Develop and own Quarterly Business Reviews in partnership with Regulatory Affairs and key strategic vendor partners.
* Create and implement a well-structured digital asset management strategy to ensure seamless organization and easy accessibility of assets.
* Collaborate with teams with varied strengths to establish efficient copy approval processes and streamline workflows.
* Take charge of implementing a sophisticated digital asset management system to improve efficiency and cultivate collaboration.
* Manage and maintain the digital asset library, ensuring accurate metadata tagging and content organization.
* Drive continuous improvement initiatives and innovation to enhance the quality and usability of digital assets and finding opportunities to optimize processes and increase productivity.
* Lead and mentor a team of dedicated software developers and engineers, encouraging a collaborative and inclusive team environment.
* Implement and champion Agile methodologies, particularly Scrum, ensuring that best practices are followed throughout the development process.
* Use tools such as JIRA to lead project workflows, sprints, and backlog efficiently.
* Collaborate closely with multi-functional teams including ProductManagement, Quality Assurance, and UX/UI Design to deliver high-quality features and enhancements.
* Ensure GxP standards are met in all deployments and technical processes.
* Partner with the Business Product team to ensure the challenges, backlog, and vendors are addressed and working efficiently
* Work with software vendor to understand and implement an innovative roadmap while balancing 'base business' and defect requirements
Qualifications
Education:
* A Bachelor's degree in Information Technology or a related field, or equivalent experience, is required.
Experience and Skills:
Required:
* Demonstrated expertise in technology productmanagement, particularly in digital asset management.
* Exceptional project management skills, with the ability to efficiently implement complex digital solutions.
* Proficiency in asset management systems and familiarity with metadata tagging.
* Strong interpersonal and collaboration skills.
* Working knowledge of system integrations and ability to communicate effectively with developers.
Preferred:
* Experience in the healthcare industry or a regulated environment.
* In-depth knowledge of copy review processes and experience in developing streamlined workflows.
* Knowledge of content management systems and digital marketing platforms.
* Familiarity with regulatory requirements for copy review in the life sciences industry.
* Experience with Aprimo, Monday.com, and/or MIRO
* Relevant certifications in technology productmanagement or digital asset management.
Other:
* Proficiency in English is required.
* This role may require up to 20% domestic travel.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via *******************/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
#JNJTech
#LI-Hybrid
Required Skills:
Digital Asset Management (DAM), ProductManagement
Preferred Skills:
The anticipated base pay range for this position is :
$122,000 to $212,750
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company's long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation -120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year Holiday pay, including Floating Holidays -13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave - 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave - 10 days Volunteer Leave - 4 days Military Spouse Time-Off - 80 hours Additional information can be found through the link below. *********************************************
$122k-212.8k yearly Auto-Apply 7d ago
Director, New Product Planning and Business Development Forecasting, Global Oncology
Takeda 4.7
Boston, MA jobs
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description Director, New Product Planning and Business Development Forecasting, Global Oncology Takeda Pharmaceutical Cambridge, MA About the role:
The Director will be a key strategic though partner to the business development and new product planning teams in creating forecasts for pipeline assets and Business Development (BD) opportunities within Takeda's Oncology Business Unit (OBU).
The individual will perform strategic market analysis for pipeline assets and BD opportunities through the integration of secondary healthcare data analytics, competitive intelligence, and primary market research, and other data inputs to create quantitative insights and facilitate key business decisions. As part of this role, the individual will be interacting regularly with working with cross functional team across commercial, clinical, medical, and access/pricing teams to perform asset evaluations.
The individual will be interacting with senior leadership of the Oncology business unit to present commercial potential and will also work closely with team members from US, Japan, and EU. The individual is expected to be able to regularly synthesize key analytical outputs in management-ready deliverables to help inform and drive strategic business decisions. In addition to strong therapeutic area knowledge, the individual is expected to have a strong grasp of incorporating insights across market research, competitive intelligence and secondary data analytics to drive the commercial assessment.
How you will contribute:
Ensure that customized, global, strategic forecasts are developed for pipeline assets and BD opportunities with assumptions based on facts and research
Collaborate with team members from commercial/NPP, market research, analytics, competitive intelligence, global pricing and market access, to make sure all relevant market insights inform the forecasts.
Lead the consensus‑building process to gain alignment and/or endorsement for forecast assumptions with the senior stakeholders and Oncology Leadership Team (OLT)
Leverage advanced analytics and integrate data available across multiple sources to enhance our understanding of market impact of the assets being considered
Lead development, training and dissemination of Long Range Forecasting and applicable templates and management summaries for all relevant oncology products to regions and local operating companies of the Oncology Business Unit
Leverage advanced analytics and integrate data available across multiple sources to enhance our understanding of market impact and as a result, Takeda's brand and business strategy.
Lead identification, maintenance, and generation of data references/databases, analogs for continuously improving oncology epidemiology and other forecast inputs, across markets
Create forecasts that are range based, identifying key risk and opportunities of the brands/assets under consideration
Serve as a strategic thought partner to the commercial/NPP teams and other key stakeholders as they work through the strategy to accelerate pipeline assets and evaluate BD opportunities
Manage and supervise a team of Takeda resources and vendors (onshore & offshore team) to deliver on key priorities
Minimum Requirements/Qualifications:
BA/BS degree, Advanced degree preferred.
Minimum of 10 years of relevant experience in forecasting, market research, or business analytics in the biopharmaceutical industry.
Significant experience conducting complex assets valuations in a fast‑paced environment.
Experience with advanced spreadsheets, patient based forecast modeling including dynamic patient models
Experience in business development forecasting, preferred
Experience in oncology, solid tumors, hem tumors or similar specialty areas
Experience with quantitative techniques including smoothing, regression, time series analyses, and simulation. Experience with data analysis and data visualization tools.
Product launch and Global experience. Consulting experience with forecasting, market research or business analysis firm(s)
Broad working knowledge of commonly used biopharmaceutical industry databases
Working knowledge of global access and reimbursement policies, and competitive environment and potential impact on product development and commercialization strategy
Ability to facilitate large meetings and influence senior stakeholders
Ability to work collaboratively in a team‑based environment, including external vendors
Demonstrated excellence in project management and effectively managing multiple projects/priorities.
Exceptional oral and written communications skills with the capacity to present effectively to a diverse range of audiences.
Ability to explain complex concepts to stakeholders in simple language and lead/drive consensus building
Demonstrated analytical skills combined with a client‑service mindset
Demonstrated ability to think strategically, identify key issues and value drivers, and translate strategic insights into an appropriate analytical framework.
More about us:
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient‑focused company that will inspire and empower you to grow through life‑changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
This position is currently classified as “hybrid” in accordance with Takeda's Hybrid and Remote Work policy.
Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location:
Boston, MA
U.S. Base Salary Range:
$174,500.00 - $274,230.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short‑term and/or long‑term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short‑term and long‑term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well‑being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations
Boston, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Job Exempt
Yes. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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$174.5k-274.2k yearly 5d ago
Product Manager (Pharmaceutical manufacturing)
HTI 4.3
Parsippany-Troy Hills, NJ jobs
HTI is assisting a large pharmaceutical manufacturing company in the Parsippany, NJ area with their search for an experienced ProductManager. This is a full-time, direct hire, hybrid position with the ability to work remotely 2 days per week, with three days per week in the office. The salary range is $100,000 - $140,000 / year, depending on experience and education.
This company offers a fun, collaborative work environment, fantastic benefits, and opportunities for growth! Relocation assistance is available for qualified candidates located in the continental U.S.
Requirements:
Bachelor's degree in Business, Finance, Supply Chain or a similar major. Master's degree or MBA is a plus.
7 or more years of recent experience in a ProductManagement role within the pharmaceutical manufacturing industry with responsibility for the job duties listed below.
Strong background in product launch planning, commercial and competitive analysis, statistical software, and forecasting techniques.
Experience utilizing pharma industry databases, including IQVIA, ProspectoRx, First Databank, and FDA Orange Book.
Knowledge of FDA regulatory requirements.
Advanced Excel and PowerPoint skills; ERP system experience (Oracle, SAP or similar)
Must be currently located in the Parsippany, NJ area or be able to relocate.
Must be authorized to work in the U.S. without visa sponsorship, both now and in the future.
Job Summary:
Provide productmanagement, modeling and commercial analysis to support product development and life cycle management. This role will manageproduct forecasting, competitive analytics, reporting, and product launch coordination. This team member's strategic forecasting and planning skills will be instrumental in optimizing inventory levels, minimizing costs, and supporting the company's overall strategic goals.
Job duties include:
Conduct product forecasting/modeling for all commercial products, which supports business case development, demand planning, manufacturing readiness, and financial budgeting.
Provide commercial business insights and reporting to support growth and commercial execution, including competitive and market share analysis, business and competitive intelligence reporting, product performance and ad hoc.
Support and coordinate the execution of new product launch plans.
Support business development modeling and modeling for new product targets.
Responsible for performing commercial analytics, insight generation and competitive analysis.
Contribute to financial quarterly planning cycle, including owning commercial re-forecasting models and supporting portfolio sales economics.
Provide overall analysis of company revenue and provide support for the finance and leadership teams in understanding portfolio changes, including those driven by the outside commercial team (BD, R&D, etc.).
Support the development of marketing materials for existing and new product launches, including sell sheets, product catalog, PR, advertising, podium, white papers, etc.
Support commercial and market assessments to drive execution of new product launches and achieve product targets.
Support the management and reporting of pipeline postmortem and launch success tracking.
Coordinate with the finance team to deliver ad hoc analysis.
Utilize statistical models, market analysis, and historical data to forecast demand for pharmaceutical products (new and existing) across different regions and markets.
Monitor forecast accuracy and key performance indicators (KPIs) to continuously improve forecasting models and processes.
Benefits include:
Medical, dental and vision coverage
401K with company match
Progressive PTO plan
Hybrid work schedule
$100k-140k yearly 6d ago
Senior Director, Access Strategy Established Products
Sanofi 4.3
Massachusetts jobs
**About the Job**The Sr Director, Transplant Market Access Strategy & Provider Accounts will lead a small team and be responsible for developing and implementing the short and long-term transplant market access strategy (positioning, pricing, contracting, pull-through plans) from start to end, for national/regional payers, institutions, channel customers, and patient support services. The candidate will utilize portfolio expertise and managed markets experience to build an integrated market access strategy based upon the brands strategies. The ability to identify key customer segments and generate customer insights is critical in this role. In addition, the role will define & implement inline and launch indication pricing strategy, MAx strategy, plan/tools, based on the global brand strategies. The incumbent will be responsible for transversally leading across diverse teams including Marketing, Market Access Shared Services, HEVA/RWE, PSS, Trade, Finance, Legal, manufacturing and logistics, and field sales. The candidate must have strong business acumen and outstanding communication and interpersonal skills to develop productive relationships across all internal and external customer groups. We are an innovative global healthcare company with a focus on immunology that extends to innovation in diabetes and transplant medicine. Across different countries, our talented teams are determined to deliver a best-in-class customer experience using the best of digital, artificial intelligence and personal know-how. With a focus on immunology that extends to innovation in diabetes and transplant medicines, we pursue progress to make a real impact on millions of patients around the world.**Main Responsibilities:*** Partner effectively with support functions, Global Market Access and US teams to execute on MAx core deliverables (ex. specific market access or other tools).* Represent the access customer perspective within cross-functional, cross-regional commercialization teams including Brand, USMA, HEVA/RWE, Market Access Shared Services, Trade, Finance, Communications, Policy/Advocacy, and Public Affairs thereby optimizing the lifecycle of transplant products.* Partner with relevant departments (as listed above) to influence the market assessment, product positioning, and target product profile by providing strategic input regarding market access, reimbursement, and pricing information throughout the product lifecycle.* Participate in account discussions, as necessary, to communicate brand value, strategies, and market dynamics as they impact the product.* As a part of the broader global market access community, work closely with access professionals across the world ensuring consistent feedback and optimization of Global Value and Access deliverables including launch preparation, negotiations training, and contracting (including value-based and outcomes-based frameworks).* Develop market access strategies for future indications including generation of pricing recommendation, value proposition and messages, and detailed forecastassumptions, support strategies within depth market research, and environmental data & analogs as appropriate.* Partner closely with marketing on the assessment of business development/divestiture opportunities.* Monitor the marketplace for market access challenges, trends, threats & opportunities.* Partner closely with market access strategy colleagues within BU and across the organization to share best practices, customer insights and emerging trends.**About You****Basic Qualifications:*** BA/BS and 10+ years' relevant professional experience including market access, health economics, pricing & reimbursement* 10+ years' experience at local and/or international level w/ knowledge of US and Global market access & payer environment* Knowledge of disease market access desirable, but other backgrounds are welcomed.**Preferred Qualifications:*** Proven track record of leading within a matrix environment to reach business objectives* Demonstrated ability to take on highly complex business problems, recommend strategic and tactical solutions in a simple and straightforward manner* Exhibits outstanding written and oral communication skills, including the ability to effectively write and deliver presentations to professionals at all levels within Sanofi* Demonstrated relationship building and team management at all levels of the organization and across geographies **Travel:*** Approximately 10-20% The successful candidate will be required to sign and execute a restricted covenant upon hire.**Why Choose Us*** Bring the miracles of science to life alongside a supportive, future-focused team.* Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.* Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.* Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.#GD-SG #LI-GZ#LI-Onsite#vhd# Pursue *progress*, discover *extraordinary*Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !*US and Puerto Rico Residents Only*Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.*North America Applicants Only*The salary range for this position is:$202,500.00 - $337,500.00All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the .**Job Title**: Senior Director, Access Strategy Established Products**Location:** Morristown, NJ or Cambridge, MA
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$202.5k-337.5k yearly 7d ago
Senior AI Product Leader - Commercial Tech (Hybrid)
Vertex Pharmaceuticals 4.6
Boston, MA jobs
A leading biotechnology company is seeking a Senior Director to lead AI ProductManagement within their organization. This role involves developing high-value AI products that enhance operations and patient access. Candidates should have over 12 years of industry experience, a strong background in AI/ML, and leadership in cross-functional settings. This role offers a hybrid work model and competitive total rewards, including flexible benefits and career support.
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$102k-141k yearly est. 6d ago
Social Media Manager
Avara 4.1
Dallas, TX jobs
Reports To: Director of Social & Acquisition / VP of Marketing & Ecomm
Type: Full-Time
About Us
Avara is a dynamic and innovative company dedicated to creating a sense of community through the shared love of fun, accessible, curated fashion that will inspire women to feel authentically confident. Avara creates and curates a line of women's clothing and accessories that come with compliments guaranteed!
Avara was founded in 2018 by a mother, Emily Wickard, who after spending 20 years in Corporate Finance, decided to take a leap of faith and start her own clothing brand. Since its humble beginnings in Emily's home, Avara has grown exponentially, with "Avaraistas" in every state and over 130,000 satisfied customers. In 2023, Avara was recognized as the #1 fastest growing privately held eCommerce company in the country by Inc Magazine.
Our goal is to be the go-to brand for fun, accessible fashion that allows women to celebrate all of life's moments with confidence and joy.
Job Overview
We're looking for a Social Media Manager who will primarily lead and run our CEO's social media presence while also overseeing the strategic direction of our brand accounts. This role is the driving force behind the CEO's voice, visibility, and thought leadership online-creating a strong, influential founder-led social presence that fuels brand credibility and growth. You will manage day-to-day content creation for the CEO, guide the brand's social direction, and ensure both channels work together in a cohesive, high-impact way.
Key Responsibilities
Social Media Ownership
Serve as the primary owner of the CEO's social media channels-managing strategy, content planning, creation, publishing, and optimization.
Oversee high-level direction for the brand social accounts, partnering with the Social Media Coordinator for execution.
Launch and grow brand TikTok account
Maintain consistent content themes, brand alignment, and differentiated voices between CEO and brand accounts.
Content Strategy & Creation
Develop and execute a robust, platform-specific content calendar for the CEO, with a strong focus on storytelling, behind-the-scenes content, industry POV, and thought leadership.
Create overall content direction for brand channels and ensure alignment with marketing initiatives.
Tailor strategies for each platform (Instagram, Facebook, TikTok, LinkedIn, Pinterest, Threads, etc.) based on audience behavior and trends.
Collaborate with the copywriter to develop compelling captions, hooks, and CTAs for both the CEO and brand accounts.
Ideate content concepts, provide creative direction, and ensure flawless end-to-end execution.
Engagement, Growth & Performance
Drive engagement, follower growth, reach, and acquisition for the CEO's account, while supporting growth programs for the brand.
Cultivate relationships with affiliates, influencers, ambassadors, and community members to support visibility and partnership opportunities.
Own content boosting for brand and CEO in partnership with Paid Specialist
Analytics & Optimization
Monitor and analyze performance across CEO and brand channels; use insights to refine strategies and inform decision-making.
Stay current on platform updates, cultural trends, and algorithm shifts to proactively evolve the content approach.
Propose and implement new ideas to accelerate growth.
Establish and maintain a clear, consistent reporting cadence.
Collaboration
Partner with marketing, design, and e-commerce teams to align content with product launches, brand moments, and campaigns.
Support influencer and UGC initiatives by coordinating content and facilitating reposts.
Work closely with the Founder/CEO to streamline content workflow, approvals, and filming opportunities.
Qualifications
3-5 years of experience in social media management, ideally within fashion, beauty, lifestyle e-commerce, or other fast-paced industries.
Deep expertise in platform-specific strategies, especially Instagram Reels, TikTok, and LinkedIn.
Exceptional writing, editing, communication, and storytelling capabilities.
Proficiency with content creation tools (e.g., Figma, Asana, CapCut).
Strong project management skills with impeccable organization.
Passion for fashion, digital culture, and developing strong founder-led content narratives.
Why You'll Love Working Here
High impact: You'll play a crucial role in scaling our paid efforts across major platforms.
Creative energy: Work with a talented in-house team + agency creatives to bring our brand to life.
Built-in structure: With so many asset and campaign moving parts, your organizational talent will shine.
Growth-focused: As we grow, you'll grow-your role and daily responsibilities will evolve with us.
$52k-74k yearly est. 3d ago
Product Manager, Analytics - Medical Affairs
Gilead Sciences, Inc. 4.5
Foster City, CA jobs
ProductManager, Analytics - Medical Affairs | United States - California - Foster City | Medical Affairs | Regular
The ProductManager, Analytics for Medical Affairs will lead the development and continuous improvement of self-serve analytics solutions that provide actionable insights to support medical affairs operations. This role focuses on building dashboards and reporting tools that enhance decision-making, optimize medical activities, and measure the impact of evidence generation and scientific engagement. The ideal candidate has extensive productmanagement expertise and a robust understanding of medical affairs processes within the pharmaceutical or life sciences industries.
Responsibilities
Develop the product roadmap for dashboards and analytics tools, aligning them with the goals of the medical affairs organization and functions.
Identify and build business cases for analytical solutions such as product launches, key initiatives, and medical education programs.
Partner with medical excellence, scientific communications, insights, and other MA teams to gather requirements, design KPIs/metrics and connect them to medical impact.
Prioritize development efforts based on business needs, user feedback, and resource availability.
Manage the entire product lifecycle from ideation to delivery and hypercare, working closely with developers, data engineers, and analysts to build and optimize dashboards using tools like Spotfire.
Ensure dashboards are intuitive, scalable, and capable of delivering real-time insights to medical affairs teams and other stakeholders.
Continuously improve product features by gathering feedback from end-users and monitoring product performance.
Establish KPIs to measure the effectiveness and impact of medical affairs activities using analytics tools.
Track solution usage and identify areas for improvement, automation, and optimization.
Ensure that dashboards and reports enable data-driven decision-making across the medical affairs function.
Ensure analytics solutions adhere to regulatory standards, such as HIPAA, GDPR, and other healthcare data privacy regulations.
Maintain high standards for data quality, accuracy, and security across all reporting tools.
Qualifications
Bachelor's degree in Data Science, Business Administration, Computer Science, or Life Sciences (MBA or advanced degree preferred).
7+ years of experience in productmanagement or analytics, with at least 3 years in a senior role within the healthcare, pharmaceutical, or life sciences industries.
Strong understanding of medical affairs processes and the pharmaceutical product lifecycle.
Expertise with BI tools such as Power BI, Tableau, Qlik, or equivalent platforms.
Familiarity with data querying languages (SQL) and cloud-based platforms (e.g., AWS, Azure).
Experience working in Agile product development environments, with proficiency in tools such as Jira or Trello.
Excellent communication and stakeholder management skills, with the ability to translate business needs into technical solutions.
Knowledge of machine learning or artificial intelligence (AI) applications in medical analytics.
Familiarity with clinical trial data and regulatory reporting requirements.
Project management certification (e.g., PMP, Scrum) is a plus.
Job Details
Job Requisition ID: R0045081
Employment Type: Full-Time
Job Level: Manager
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$110k-142k yearly est. 7d ago
Product Quality Director - Synthetics
Amgen Sa 4.8
Thousand Oaks, CA jobs
Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas-Oncology, Inflammation, General Medicine, and Rare Disease-we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller, happier lives.
What you will do
Let's do this. Let's change the world.
In this vital role you will be the champion for a product team as the Product Quality Leader (referred to as PQL), providing technical expertise, strategic and project leadership to the Product Quality (PQ) organization. The PQL has responsibility for working with PQ staff and executive leadership, International Quality, Quality Control, Contract Manufacturing Quality, Regulatory, Process Development, Quality Assurance, and other functional areas on the resolution of issues associated with process/manufacturing, in process controls, analytical methods, specifications, reference standards, importation testing, investigations, change control, regulatory submissions and inspections. The PQL has responsibility for driving change to implement operationally efficient processes and corporate alignment across international sites. As a leader in Product Quality, the successful candidate is expected to have experience, knowledge and understanding of small molecule, peptide, and/or oligonucleotide development and commercial lifecycle maintenance, product stability programs, CMC regulatory filings, risk assessment, and Amgen Quality Management Systems.
Amgen offers the opportunity to be at the interface between research, global development and manufacturing to ensure that our molecules become medicines. Many of the technologies we're employing are not only new to Amgen but are new to the industry as a whole. Help us to pave new roads for patients.
This role is directly responsible for the product quality and related activities (e.g., comparability, specifications, stability, annual product review) in support of the Product Development Team (PDT). The PQL provides scientific oversight for the product quality of pivotal and/or commercial product(s) including timely product data review, ownership of GMP documents and regulatory filing sections, execution of transactions in relevant GMP system, and support for regulatory audits and responses to questions. The individual is directly responsible for leading a Product Quality Team (PQT), including oversight of the product stability programs, providing indirect staff management and guidance to members of the PQT.
Responsibilities
Provide effective, cross-functional quality leadership, and manage multiple, complex long-term PDT deliverables for late phase and commercial programs, including actions required for the PQT/APR; specification, comparability, and stability programs; site and method transfers; product quality impact statements for NCs; and PQ owned regulatory filing sections and RTQs
Provide expertise in science and risk-based evaluation of complex processes and product quality data, including ability to develop patient-oriented strategies that account for business needs and/or provide novel solutions to complex issues
Demonstrate proficiency in oral and written communication of complex information to Amgen leadership, peers and regulatory agencies including communications associated with inspectional activities
Demonstrate proficiency in knowledge of cGMP and international regulatory expectations
Understand and respond to the impact of emerging scientific/technical trends and their implications for Amgen
Actively mentor new and existing team members to develop Product Quality core skills
Qualifications Basic Qualifications
Bachelor's Degree and 9 years of Quality, Operations, Scientific, or Manufacturing experience OR
Master's Degree and 7 years of Quality, Operations, Scientific, or Manufacturing experience OR
Doctorate Degree and 4 years of Quality, Operations, Scientific, or Manufacturing experience
Preferred Qualifications
Advanced degree in chemistry, biochemistry, biology, or a related biotechnology sciences field
Expertise in the areas of drug substance and drug product manufacturing, analytical testing, and industry regulations related to small molecules, peptides and/or oligonucleotides.
8+ years of pharmaceutical experience with increasing responsibility in quality, analytical development, process development, pharmaceutics, regulatory, or manufacturing environment experience
6+ years working in a regulated environment (direct GMP)
4 years experience managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources
2+ years experience as a technical expert or product champion
1+ years of experience with authoring or review of regulatory filing or similar regulatory documentation.
1+ years of experience supporting non-conformance investigations, authoring, reviewing and defending critical product impacting non-conformances
Experience in Project Management in support of product development
Knowledge of quality, compliance and regulatory requirements
Knowledge of analytical techniques used for synthetic product quality control
Understanding of drug substance and drug product development and manufacturing
Strong leadership and management skills
General knowledge of cGMP and filing regulations, practices, and trends pertaining to the manufacture and testing of pharmaceuticals
Previous experience working on a cross-functional team in a matrix environment
Excellent written and verbal communication skills, including facilitation and presentation skills
Benefits
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
Sponsorship for this role is not guaranteed.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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$161k-211k yearly est. 5d ago
Sr. Director Global Omnichannel Marketing Product Management
Gilead Sciences, Inc. 4.5
Foster City, CA jobs
Sr. Director Global Omnichannel Marketing Next Best Action ProductManagementUnited States - California - Foster City Commercial/Sales Operations Regular
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**This role will be based in Foster City CA
Key Responsibilities
Global position supporting multiple countries across several brands leading and shaping our AI/ML enabled Omnichannel marketing solution to deliver increased ROI.
Directly liaise with countries to ensure our capabilities are well positioned and leveraged with in-country marketing and operations teams.
Identify and prioritize short- and long-term opportunities for the omnichannel product, and drive product strategies and roadmaps in alignment with product strategic goals
Effectively communicate technical concepts to diverse audiences to drive user adoption and satisfaction
Leverage metrics to evaluate overall product performance, and work with countries to drive content personalization.
Conduct Market Research using (but not limited to) Behavioral Science frameworks to understand humanistic biases/attitudes in Gilead Customers that can ultimately be leveraged for content personalization and perception change.
Leverage existing segments to provide additional insights and incremental knowledge on customer attitudes and behaviors.
Provide insights and support development of content journeys for microsegments across markets by partnering with country marketing teams.
Documentation & Knowledge Base: Support the development of comprehensive documentation and maintain a knowledge base to ensure business continuity, retain intellectual property, and facilitate information sharing.
Vendor Management: Proactively manage and optimize business vendor relationships, oversee contract negotiations, and ensure consistent performance and delivery to support operational needs and strategic goals.
Cross-Functional Collaboration: Collaborate closely with Market Insights (Global and Regional), IT, Marketing, Sales, and Analytics teams, to integrate DCI insights into NBA implementation, Marketing Strategies and content.
Budget Management & Resource Allocation: Manage project budget to agreed financial target and effectively allocate resources to ensure optimal utilization and alignment with organizational objectives.
Data Governance and Ethics: Ensure compliance with data privacy regulations (such as GDPR and HIPAA) and uphold the highest standards of data ethics.
Required
14+ Years with BS/BA
12+ Years with MS/MA or MBA
Preferred Experience
Relevant experience in biotechnology, pharmaceuticals, or consulting with a focus in one or more areas of marketing, market research, forecasting, analytics, decision analytics, commercial strategy.
Experience with Omnichannel Marketing content personalization/Analytics/Market research
Prior experience conducting, analyzing, and communicating qualitative and quantitative market research.
Must possess good task management skills, planning, prioritization, objective setting, and meeting management and plan execution
History of working and delivering on multiple projects simultaneously, with tight deadlines and changing priorities is required
Exceptional written and verbal communication skills are required
Experience in successfully presenting to senior leadership audiences, including simplifying complex materials, educating, and managing audiences with differing viewpoints to get to alignment via clear and compelling storylines
Experience in biopharmaceutical-focused marketing, commercial strategy, or consulting is desirable.
Business leadership experience, and a track record of “influencing without authority” (specifically, more senior Commercial and cross-functional partners) in successful conflict resolution and driving consensus.
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
Job Description
Role: Sr. Director Global Omnichannel Marketing Next Best Action ProductManagement
**This role will be based in Foster City CA
Key Responsibilities
Global position supporting multiple countries across several brands leading and shaping our AI/ML enabled Omnichannel marketing solution to deliver increased ROI.
Directly liaise with countries to ensure our capabilities are well positioned and leveraged with in-country marketing and operations teams.
Identify and prioritize short- and long-term opportunities for the omnichannel product, and drive product strategies and roadmaps in alignment with product strategic goals
Effectively communicate technical concepts to diverse audiences to drive user adoption and satisfaction
Leverage metrics to evaluate overall product performance, and work with countries to drive content personalization.
Conduct Market Research using (but not limited to) Behavioral Science frameworks to understand humanistic biases/attitudes in Gilead Customers that can ultimately be leveraged for content personalization and perception change.
Leverage existing segments to provide additional insights and incremental knowledge on customer attitudes and behaviors.
Provide insights and support development of content journeys for microsegments across markets by partnering with country marketing teams.
Documentation & Knowledge Base: Support the development of comprehensive documentation and maintain a knowledge base to ensure business continuity, retain intellectual property, and facilitate information sharing.
Vendor Management: Proactively manage and optimize business vendor relationships, oversee contract negotiations, and ensure consistent performance and delivery to support operational needs and strategic goals.
Cross-Functional Collaboration: Collaborate closely with Market Insights (Global and Regional), IT, Marketing, Sales, and Analytics teams, to integrate DCI insights into NBA implementation, Marketing Strategies and content.
Budget Management & Resource Allocation: Manage project budget to agreed financial target and effectively allocate resources to ensure optimal utilization and alignment with organizational objectives.
Data Governance and Ethics: Ensure compliance with data privacy regulations (such as GDPR and HIPAA) and uphold the highest standards of data ethics.
Required
14+ Years with BS/BA
12+ Years with MS/MA or MBA
Preferred Experience
Relevant experience in biotechnology, pharmaceuticals, or consulting with a focus in one or more areas of marketing, market research, forecasting, analytics, decision analytics, commercial strategy.
Experience with Omnichannel Marketing content personalization/Analytics/Market research
Prior experience conducting, analyzing, and communicating qualitative and quantitative market research.
Must possess good task management skills, planning, prioritization, objective setting, and meeting management and plan execution
History of working and delivering on multiple projects simultaneously, with tight deadlines and changing priorities is required
Exceptional written and verbal communication skills are required
Experience in successfully presenting to senior leadership audiences, including simplifying complex materials, educating, and managing audiences with differing viewpoints to get to alignment via clear and compelling storylines
Experience in biopharmaceutical-focused marketing, commercial strategy, or consulting is desirable.
Business leadership experience, and a track record of “influencing without authority” (specifically, more senior Commercial and cross-functional partners) in successful conflict resolution and driving consensus.
The salary range for this position is: $243,100.00 - $314,600.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
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* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
For jobs in the United States:
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex , age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
PAY TRANSPARENCY NONDISCRIMINATION PROVISION
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
For Current Gilead Employees and Contractors:
Please apply via the Internal Career Opportunities portal in Workday.
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Job Requisition ID R0046084
Full Time/Part Time Full-Time
Job Level Director
Remote Type Onsite Required
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$243.1k-314.6k yearly 3d ago
Senior Product Manager, HIV Prevention, DTC Marketing
Gilead Sciences, Inc. 4.5
Foster City, CA jobs
As a SeniorProductManager, HIV Prevention DTC Marketing, you will support and execute both Branded and PrEP education tactics focused on reaching and engaging Individuals that need or want PrEP. This SeniorProductManager will report directly to the Senior Director, HIV Prevention DTC Marketing.
This role is based in Foster City, CA, requiring on-site presence three days a week; remote or off-site work is not permitted.
Responsibilities
Support and manage key tactical executions related to US HIV Prevention/PrEP Consumer initiatives, including online and offline Branded tactics as well as Unbranded PrEP education tactics.
Develop and implement content and messaging directed towards diverse Consumer groups, including men who have sex with men, cis-gender women and transgender individuals across different race and ethnicities.
Demonstrate proficiency in traditional and innovative marketing channels, including TV, digital, audio, social media, print, point-of-care, out-of-home and CRM and support the execution of creative assets development across these channels.
Help lead the development of Consumer tactics according to overall business strategy and within agreed upon budgets.
Work collaboratively with cross functional partners throughout development of tactics, help solve business problems and create efficiencies across DTC efforts.
Effectively manage multiple agency partners to produce deliverables within timelines and allocated budget.
Gain approval for marketing materials through internal review process to ensure marketing activities are in compliance with medical, regulatory and legal requirements.
Develop and deliver presentations to a range of internal stakeholders and external audiences
Basic Qualifications
Bachelor's Degree and Eight Years' Experience
OR
Masters' Degree and Six Years' Experience
Preferred Qualifications
Bachelor's degree in marketing or related field and eight years of work experience or Masters' degree and six years of work experience.
A minimum of 3 years in product marketing or advertising focused on Consumers or patients.
Strong familiarity with marketing fundamentals, promotional strategy, and commercial policies and practices.
Previous experience in marketing, market research and/or advertising/communications agency experience desired.
Possess strong interpersonal skills with ability to collaborate effectively and drive consensus among internal and external cross-functional partners
Demonstrate project management skills, tactical development, planning, execution, and prioritization among competing business needs.
Excellent communications skills with an ability to efficiently and productively communicate both orally and in writing are required.
Ability to think critically through complex business problems, offer solutions and clear point of view.
Demonstrated understanding of pharmaceutical regulatory requirements and impact on development of marketing materials.
Proficient in budget and timeline management
Thrives in a fast‑paced, dynamic environment
Listens carefully to other points of view and is able to adapt style and content based on audience
Must be comfortable with discussing HIV/HIV Prevention category, including topics related to sex and sexual identity.
People Leader Accountabilities
Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
Develop Talent - understand the skills, experience, aspirations, and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop, and realize their purpose.
Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.
Job Requisition ID R0044563
Full Time/Part Time Full-Time
Job Level Manager
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$136k-175k yearly est. 3d ago
Senior Manager of Marketing - Yescarta
Gilead Sciences, Inc. 4.5
Santa Monica, CA jobs
We are seeking a highly motivated individual to join us as the SeniorManager of Marketing - Yescarta focused on the LBCL indication. The SeniorManager of Marketing will play an important role in translating the LBCL brand strategy into prioritized, measurable HCP tactics, partnering crossfunctionally to deliver highquality execution that supports and grows Yescarta's LBCL indication. This person will report to the Senior Director, LBCL within Kite's US Commercial Department.**Key Responsibilities of the SeniorManager** **of Marketing -** ****Yescarta** **in**clude:**Guide the development and delivery of differentiated brand materials, ensuring content reflects the brand's purpose and customer needs while staying grounded in evidence and label. Exhibit a "roll up your sleeves" attitude, demonstrating the ability to follow through on projects within tight timelines. OR OR OR OR High School Diploma / GED degree and 12+ years of experience**Basic Qualifications:** Doctorate and 2+ years of experience Master's degree and 6+ years of experience Bachelor's degree and 8+ years of experience Associate degree and 10+ years of experience6+ years of pharmaceutical or biotechnology experience Experience in marketing research and / or pharmaceutical sales Prior hematology / oncology or cell therapy experience Ability to leverage data to conduct analyses and use complex analytical tools to drive decisions Ability to successfully work with external agencies, including advertising, public relations and medical education vendors to develop programs and materials Familiarity with marketing fundamentals, strategy, sales and commercial policies and practices Everyone at Kite is grounded by one common goal - curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work.
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$131k-161k yearly est. 3d ago
Senior HIV Prevention DTC Marketing Manager
Gilead Sciences, Inc. 4.5
Foster City, CA jobs
A leading biopharmaceutical company is seeking a SeniorProductManager for HIV Prevention within its DTC Marketing team in Foster City, CA. This role involves managing marketing tactics to engage diverse consumer groups, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams. The ideal candidate will have extensive marketing experience, strong project management skills, and the ability to thrive in a dynamic environment. This is a full-time position requiring on-site presence three days a week.
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$133k-164k yearly est. 3d ago
Principal Product Manager, AI & Digital Health
Tandem Diabetes Care 4.6
Highland, CA jobs
GROW WITH US: Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We'd love for you to team up with us to “innovate every day,” put “people first,” and take the “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry.
STAY AWESOME:
Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology - an advanced predictive algorithm that automates insulin delivery. But we're so much more than that. Our company's human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com
A DAY IN THE LIFE:
The Principal ProductManager, AI & Digital Health, drives the evolution of our digital ecosystem with a dual focus: shaping AI-driven platform capabilities and leading a near-term advanced technology initiative - a mobile app for next generation therapy. This role sets the vision and roadmap for intelligent features and advanced data services across our digital product suite while taking immediate product ownership of a modern, mobile application designed to advance therapy options for people with diabetes.
This role is ideal for an entrepreneurial leader who thrives on pioneering new product concepts, and bringing innovative products to market. You will have an opportunity to make an immediate impact delivering a strategic mobile product this year while establishing the vision, strategy, and foundations for Tandem's AI capabilities. Success requires creativity in solving complex problems, excellent communication skills, and the ability to navigate ambiguity while clearly defining a path forward. You are skilled at influencing and motivating teams to deliver meaningful outcomes.
The Principal ProductManager, AI & Digital Health, at Tandem is also responsible for:
AI Product & Platform Management
Owns and communicates the vision and strategy for AI-driven innovations across Tandem's digital ecosystem, ensuring alignment with business objectives and user needs.
Develops and maintains product roadmaps that integrate ambient intelligence and advanced AI capabilities-such as conversational assistants, summarization and insights, anomaly detection, and agentic workflows-into intuitive experiences across mobile, cloud, and embedded platforms.
Translates business and market requirements into clear strategic priorities and actionable user requirements.
Partners with Product peers and cross-functional teams-including Engineering, Data Science, Design, Quality, Clinical, and Regulatory-to deliver AI capabilities that enhance patient and clinician experiences.
Leads the design, development, and deployment of complex and novel AI features, as well as frameworks for AI evaluation, experimentation, and A/B testing to drive data-informed decisions.
Communicates product lifecycle updates, roadmap iterations, and performance insights to senior and executive leadership with clarity and strategic context.
Proactively addresses business, regulatory, and strategic challenges; recommends improvements to mitigate risks and accelerate success.
Removes strategic and operational obstacles that hinder team performance and achievement of goals.
Establishes mechanisms to measure AI feature performance, evolution, safety, usability, and clinical impact, ensuring alignment with human factors, quality, and regulatory processes (including FDA Predetermined Change Control Plans) and ethical standards.
Leverages data, experimentation, and emerging AI technologies to inform product decisions and roadmaps, driving continuous innovation and iterative improvement.
Sets success metrics and long-term strategic plans for AI-enabled products and platforms.
Acts as an internal champion and subject matter expert for AI capabilities and their role in Tandem's product strategy.
Monitors and analyzes metrics that inform product success, including Key Performance Indicators (KPIs).
Creates governance frameworks and standards for data infrastructure and services (e.g., attribute service) to enable scalable, secure, and efficient support of ML/AI/LLM models and agentic workflows.
Mobile Product Owner - Advanced Technology Program
Accountable for ensuring that team actions and backlog are consistently aligned to the program roadmap, ongoing insights and user needs, and delivery against key milestones.
Document product requirements in line with product strategy and collaborate closely with Product, UXD/UXR, R&D, Quality, and other partner teams to ensure backlog contains the necessary detail to ensure efficient prioritization, development, testing, and deployment.
Regularly prioritizes, monitors and tracks progress of the team backlog and business commitments, communicating this with the team to manage expectations and set delivery targets to achieve program objectives.
Leads backlog refinement and sprint review sessions, while joining other sprint and program events as an active participant and product leader.
Balances new product and feature development equally with technical debt, bugs, and anomalies and able to articulate business and technical rationale for decisions.
WHEN & WHERE YOU'LL WORK:
This role will be a mix of in-office work at our corporate headquarters in Del Mar, CA and remote work. This position is expected to be in office on as needed basis but may vary depending on business demands.
WHAT YOU'LL NEED:
8+ years productmanagement experience, including leadership of digital or mobile products and AI-based product development.
Bachelor's degree in Computer Science, Engineering, Mathematics or related field.
Experience with diabetes related products, therapies, and technologies
Experience with AI model evaluation frameworks with regulated digital health systems.
Strong leadership and communication skills; adept at influencing cross-functional teams and navigating ambiguity.
Proven success developing and launching AI/ML-powered products across full product lifecycle (0-to-1, 1-to-n, “cradle-to-grave”) with strong AI evaluation definition, development and compliance experience.
Expertise in agile product development processes, product ownership responsibilities.
Experience managing integrated systems encompassing hardware & software components; strong knowledge of underlying technologies and methods including machine learning.
Communicates complex ideas, anticipates potential objections and influences others, often at senior levels, to adopt a different point of view.
Hands-on experience with Agile software development methodology.
Solves unique problems with broad impact on the business.
Demonstrated ability to build trust and engage engineering teams through the product development process.
Anticipates clinical and regulatory issues as it relates to delivering software as a medical device.
Skilled at clearly conveying in-depth knowledge to all levels within, and outside of, the organization.
Ability to operate effectively in a matrixed environment and establish cooperative relationships with peers and key functional owners.
EXTRA AWESOME:
MBA, preferred.
Certified Scrum Product Owner (CSPO) certification preferred
General understanding of the diabetes industry; direct experience preferable.
COMPENSATION & BENEFITS:
The starting base pay range for this position is $176K - $205k annually. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate's location and the overall job market. In addition to base pay, Tandem offers a competitive compensation package that includes bonus and a robust benefits package.
YOU SHOULD KNOW:
Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information.
Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders.
SPONSORSHIP:
We welcome applicants who currently hold valid H-1B status (transfers, extensions, or amendments). Please note that we are not considering candidates who require new H-1B cap lottery sponsorship at this time
.
WHY YOU'LL LOVE WORKING HERE:
At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at ***************************************
BE YOU, WITH US!
We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don't meet 100% of a job description's criteria - maybe you're feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us.
Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone.
REFERRALS:
We love a good referral! If you know someone who would be a great fit for this position, please share!
APPLICATION DEADLINE:
The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications.
Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow.
#LI-Remote #LI-KL1
$176k-205k yearly Auto-Apply 22d ago
Manager, Business Analyst Patient Operations Product Team
Bristol-Myers Squibb 4.6
New Brunswick, NJ jobs
Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
Bristol-Myers Squibb (BMS) seeks an experienced full-time Manager - Patient Operations Business Analyst with expertise in Salesforce technologies to manage requirements, gap analysis, and documentation for the Global Patient Services application, including translation strategy for Cell Therapy 360 portals. The role involves collaboration with diverse internal and offshore teams, functional verification, defect triage, GxP documentation, and mentoring. Candidates should have a bachelor's degree in computer science or related fields (master's preferred), 5-7 years of IT project experience, 3+ years with Salesforce, and preferably 2+ years in the pharmaceutical industry, along with skills in communication, global team management, and Agile methodologies. Salesforce certifications are a plus.
Position: Manager - Business Analyst Patient Operations Product team
BMS is looking for a full time, experienced Patient Services Business Analyst with prominent experience on Salesforce technologies. Patient Services Functional Analyst will be responsible for requirements, gap / impact analysis, translation and documentation of new features required on Global Patient Services application built on Salesforce. This role will be responsible for strategy to translate Cell Therapy 360 portals in different languages.
Key Responsibilities
· Collaborate regularly with a diverse range of internal teams including scheduling, partners, productmanagement and provide guidance on documenting business requirements in user stories.
· Requirement gap analysis and contribute to user stories functional risk assessment.
· Functional verification of user stories before passing it to the testing team.
· Collaborate with BMS Hyderabad team on user stories, requirements clarification, in-sprint refinement, sprint demos.
· Collaborate with technical and integration team on integration mapping.
· Salesforce and Integration defect triage and helping technical resources on defect management.
· Assess user stories with deep understanding of salesforce and assign appropriate size and complexity
· Author GxP documentation like configuration specification, data dictionary, user access and permissions as well as contribute to user requirement specification.
· Assess new requirement impacts to translation and manage end to end translation process from IT.
· Build strategy and execution for translating cell therapy 360 portals into new languages / markets.
· Collaborate with production support team on priority defects.
· Mentor and guide the team on requirement management, sprint & release demos.
· Keeps continuous improvement and process efficiencies in mind when evaluating releases and enhancements.
Education
· Bachelor's degree: degree in computer science, management information systems or related field.
· Master's degree preferred.
Work Experience
· 5-7 years of experience in IT project execution and/or business consulting on large enterprise implementations.
· 3+ years of experience in Salesforce Technology as Functional / Business Analyst and having exposure to Salesforce configurations.
· At least 2+ years of experience working in pharmaceutical industry is preferred.
· Experience working with Onsite and Offshore teams.
· Experience on systems supporting multi-product, multi-regions scheduling would be a plus.
· Experience on GxP systems Is preferred.
· Salesforce Certified Administrator or Advanced Administrator certification(s) a plus.
· Ability to work in Scrum team and good knowledge of Agile methodologies
Certifications
· Salesforce Certified Service Cloud Consultant certification(s) a plus.
Skills/abilities
· Excellent written and verbal communication skills, interpersonal and collaborative skills.
· Ability to communicate complex information and concepts to audiences at all levels in business and technical teams.
· Ability to manage a global team in a matrix organization.
· Ability to manage a complex vendor environment.
· Experience with Salesforce Platform.
· Experience with SDLC methodologies (Agile, SCRUM).
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
New Brunswick - NJ - US: $94,180 - $114,124 Princeton - NJ - US: $94,180 - $114,124
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit *************************************
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to **************************. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: *********************************************
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at *****************************************
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at ********************. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1597959 : Manager, Business Analyst Patient Operations Product Team
$94.2k-114.1k yearly Auto-Apply 5d ago
Manager, Business Analyst Patient Operations Product Team
Bristol Myers Squibb 4.6
Princeton, NJ jobs
Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
Bristol-Myers Squibb (BMS) seeks an experienced full-time Manager - Patient Operations Business Analyst with expertise in Salesforce technologies to manage requirements, gap analysis, and documentation for the Global Patient Services application, including translation strategy for Cell Therapy 360 portals. The role involves collaboration with diverse internal and offshore teams, functional verification, defect triage, GxP documentation, and mentoring. Candidates should have a bachelor's degree in computer science or related fields (master's preferred), 5-7 years of IT project experience, 3+ years with Salesforce, and preferably 2+ years in the pharmaceutical industry, along with skills in communication, global team management, and Agile methodologies. Salesforce certifications are a plus.
Position: Manager - Business Analyst Patient Operations Product team
BMS is looking for a full time, experienced Patient Services Business Analyst with prominent experience on Salesforce technologies. Patient Services Functional Analyst will be responsible for requirements, gap / impact analysis, translation and documentation of new features required on Global Patient Services application built on Salesforce. This role will be responsible for strategy to translate Cell Therapy 360 portals in different languages.
Key Responsibilities
* Collaborate regularly with a diverse range of internal teams including scheduling, partners, productmanagement and provide guidance on documenting business requirements in user stories.
* Requirement gap analysis and contribute to user stories functional risk assessment.
* Functional verification of user stories before passing it to the testing team.
* Collaborate with BMS Hyderabad team on user stories, requirements clarification, in-sprint refinement, sprint demos.
* Collaborate with technical and integration team on integration mapping.
* Salesforce and Integration defect triage and helping technical resources on defect management.
* Assess user stories with deep understanding of salesforce and assign appropriate size and complexity
* Author GxP documentation like configuration specification, data dictionary, user access and permissions as well as contribute to user requirement specification.
* Assess new requirement impacts to translation and manage end to end translation process from IT.
* Build strategy and execution for translating cell therapy 360 portals into new languages / markets.
* Collaborate with production support team on priority defects.
* Mentor and guide the team on requirement management, sprint & release demos.
* Keeps continuous improvement and process efficiencies in mind when evaluating releases and enhancements.
Education
* Bachelor's degree: degree in computer science, management information systems or related field.
* Master's degree preferred.
Work Experience
* 5-7 years of experience in IT project execution and/or business consulting on large enterprise implementations.
* 3+ years of experience in Salesforce Technology as Functional / Business Analyst and having exposure to Salesforce configurations.
* At least 2+ years of experience working in pharmaceutical industry is preferred.
* Experience working with Onsite and Offshore teams.
* Experience on systems supporting multi-product, multi-regions scheduling would be a plus.
* Experience on GxP systems Is preferred.
* Salesforce Certified Administrator or Advanced Administrator certification(s) a plus.
* Ability to work in Scrum team and good knowledge of Agile methodologies
Certifications
* Salesforce Certified Service Cloud Consultant certification(s) a plus.
Skills/abilities
* Excellent written and verbal communication skills, interpersonal and collaborative skills.
* Ability to communicate complex information and concepts to audiences at all levels in business and technical teams.
* Ability to manage a global team in a matrix organization.
* Ability to manage a complex vendor environment.
* Experience with Salesforce Platform.
* Experience with SDLC methodologies (Agile, SCRUM).
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
New Brunswick - NJ - US: $94,180 - $114,124
Princeton - NJ - US: $94,180 - $114,124
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit *************************************
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
* Health Coverage: Medical, pharmacy, dental, and vision care.
* Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
* Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off
* US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
* Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
* Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to **************************. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: *********************************************
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at *****************************************
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at ********************. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1597959 : Manager, Business Analyst Patient Operations Product Team
$94.2k-114.1k yearly Auto-Apply 4d ago
Manager, Business Analyst Patient Operations Product Team
Bristol Myers Squibb 4.6
Princeton, NJ jobs
**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
Bristol-Myers Squibb (BMS) seeks an experienced full-time Manager - Patient Operations Business Analyst with expertise in Salesforce technologies to manage requirements, gap analysis, and documentation for the Global Patient Services application, including translation strategy for Cell Therapy 360 portals. The role involves collaboration with diverse internal and offshore teams, functional verification, defect triage, GxP documentation, and mentoring. Candidates should have a bachelor's degree in computer science or related fields (master's preferred), 5-7 years of IT project experience, 3+ years with Salesforce, and preferably 2+ years in the pharmaceutical industry, along with skills in communication, global team management, and Agile methodologies. Salesforce certifications are a plus.
**Position: Manager - Business Analyst Patient Operations Product team**
BMS is looking for a full time, experienced Patient Services Business Analyst with prominent experience on Salesforce technologies. Patient Services Functional Analyst will be responsible for requirements, gap / impact analysis, translation and documentation of new features required on Global Patient Services application built on Salesforce. This role will be responsible for strategy to translate Cell Therapy 360 portals in different languages.
**Key Responsibilities**
· Collaborate regularly with a diverse range of internal teams including scheduling, partners, productmanagement and provide guidance on documenting business requirements in user stories.
· Requirement gap analysis and contribute to user stories functional risk assessment.
· Functional verification of user stories before passing it to the testing team.
· Collaborate with BMS Hyderabad team on user stories, requirements clarification, in-sprint refinement, sprint demos.
· Collaborate with technical and integration team on integration mapping.
· Salesforce and Integration defect triage and helping technical resources on defect management.
· Assess user stories with deep understanding of salesforce and assign appropriate size and complexity
· Author GxP documentation like configuration specification, data dictionary, user access and permissions as well as contribute to user requirement specification.
· Assess new requirement impacts to translation and manage end to end translation process from IT.
· Build strategy and execution for translating cell therapy 360 portals into new languages / markets.
· Collaborate with production support team on priority defects.
· Mentor and guide the team on requirement management, sprint & release demos.
· Keeps continuous improvement and process efficiencies in mind when evaluating releases and enhancements.
**Education**
· Bachelor's degree: degree in computer science, management information systems or related field.
· Master's degree preferred.
**Work Experience**
· 5-7 years of experience in IT project execution and/or business consulting on large enterprise implementations.
· 3+ years of experience in Salesforce Technology as Functional / Business Analyst and having exposure to Salesforce configurations.
· At least 2+ years of experience working in pharmaceutical industry is preferred.
· Experience working with Onsite and Offshore teams.
· Experience on systems supporting multi-product, multi-regions scheduling would be a plus.
· Experience on GxP systems Is preferred.
· Salesforce Certified Administrator or Advanced Administrator certification(s) a plus.
· Ability to work in Scrum team and good knowledge of Agile methodologies
**Certifications**
· Salesforce Certified Service Cloud Consultant certification(s) a plus.
**Skills/abilities**
· Excellent written and verbal communication skills, interpersonal and collaborative skills.
· Ability to communicate complex information and concepts to audiences at all levels in business and technical teams.
· Ability to manage a global team in a matrix organization.
· Ability to manage a complex vendor environment.
· Experience with Salesforce Platform.
· Experience with SDLC methodologies (Agile, SCRUM).
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
**Compensation Overview:**
New Brunswick - NJ - US: $94,180 - $114,124
Princeton - NJ - US: $94,180 - $114,124
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit *************************************
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
+ **Health Coverage:** Medical, pharmacy, dental, and vision care.
+ **Wellbeing Support:** Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
+ **Financial Well-being and Protection:** 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
**Work-life benefits include:**
Paid Time Off
+ US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
+ Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
***Eligibility Disclosure:** T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
**Uniquely Interesting Work, Life-changing Careers**
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
**On-site Protocol**
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
**Supporting People with Disabilities**
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to ************************** . Visit careers.bms.com/ (****************************************** eeo-accessibility to access our complete Equal Employment Opportunity statement.
**Candidate Rights**
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: *********************************************
**Data Protection**
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at **************************************** .
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at ******************** . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1597959 : Manager, Business Analyst Patient Operations Product Team **Company:** Bristol-Myers Squibb
**Req Number:** R1597959
**Updated:** 2026-01-11 03:50:04.456 UTC
**Location:** New Brunswick-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
$94.2k-114.1k yearly Easy Apply 3d ago
Digital Product Lead - iCare Connect
Sanofi Group 4.3
Cambridge, MA jobs
**Job Title:** Digital Product Lead - iCare Connect **Grade:** L3 **About the Job** Ready to push the limits of what's possible? Join Sanofi in one of our corporate functions and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world.
At Sanofi, we're committed to providing the next-gen healthcare that patients and customers need. It's about harnessing data insights and leveraging AI responsibly to search deeper and solve sooner than ever before.
**Sanofi** (NYSE: SNY) is a leading global integrated healthcare company that discovers, develops, and distributes therapeutic solutions to improve the lives of everyone. The company works to prevent and treat the diseases of today, as well as those we may face tomorrow. With over 100,000 dedicated professionals in more than 100 countries, Sanofi is devoted to advancing healthcare around the world.
Sanofi is an **equal opportunity employer** that embraces diversity to foster positive, innovative thinking that will benefit people worldwide. Sanofi is also committed to employing qualified individuals with disabilities and, where warranted, will provide reasonable accommodation to applicants, as well as its employees.
Sanofi operates across multiple therapeutic areas including General Medicines, Specialty Care, Vaccines and Consumer Healthcare. The role of Digital ProductManager will focus on Sanofi's Specialty Care (externally known as Sanofi Genzyme). Specialty Care focuses on rare diseases, rare blood disorders, multiple sclerosis, oncology, and immunology. We help people with debilitating and complex conditions that are often difficult to diagnose and treat. Our approach is shaped by our experience developing highly specialized treatments and forging close relationships with physician and patient communities. We are dedicated to discovering and advancing new therapies, providing hope to patients and their families around the world. Learn more at **********************
**The Global Digital Team for Specialty Care** is focused on driving and accelerating digital transformation via delivery of digital products (marketing technology platforms, digital therapeutics, etc.) across the different therapeutic areas and directed at patients, physicians and/or payers. This team works to implement Sanofi's Digital strategy by bringing dedicated expertise internally at Sanofi and externally with digital health and/or technology partners to build the core digital foundation and drive growth thru digital across all business areas.
The **Digital Product Owner, iCare** is responsible for the successful design, build, and implementation of Sanofi's digital product line focused on patient support. Some of the products in the product line include, iCareConnect (Salesforce HealthCloud), iCareMarketing (Salesforce Marketing Cloud) and iCareEvents (Veeva Events Management). We have various therapeutic areas within Sanofi's specialty care division already live in the ecosystem while we are working on bringing a few other therapeutic areas on. In this role, the DPO will collaborate with the therapeutic area business leads and other digital product owners on the team to design, build, and implement a solution using Agile methodology. Strong collaboration and understanding across stakeholders will be critical to ensure iCare supports the needs of relevant cross-functional business partners in an efficient manner. The candidate must be solution-oriented, operationally savvy, creative, highly organized, flexible, and adept at working with multiple matrix teams, including external vendors.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
**Main Responsibilities:**
+ Responsible for helping with the product backlog with a goal to deliver on commitments on time, on budget and in line with business requirements
+ Collaborates with business product owners and iCare users to understand and document user flows and processes to ensure that the voice of the customer is incorporated into the product design
+ Works cross functionally across the digital organization specially with other digital product owners as well as customer experience team
+ Document and prioritize product specifications including goals, use cases, user stories, and business requirements
+ Continuously develops and communicates the value to the development teams and defines the features of the system
+ Contributes to the definition and maintains the Non-Functional Requirements (NFRs) to help ensure that the solution meets relevant standards and other system quality requirements
+ Manages the flow of work through the program Kanban and into the program backlog
+ Collaborates with other product owners for release management through the hypercare phase
+ Comfortable consulting with cross functional partners like legal, compliance, quality when needed
**About You**
**Qualifications:**
+ Bachelor's degree.
+ 2-3 years of experience in business analysis; experience preferably on the patient services side preferred.
+ Demonstrated strong communication skills and customer service mindset
+ Completed training or certification in agile.
+ 1 year of Salesforce experience
**Preferences:**
+ Experience with Marketing Cloud, Experience Cloud, Veeva Events
+ Demonstrated ability to work collaboratively as part of a matrix team
+ Proven ability to lead and influence teams without direct authority
+ Patient Support Services or other bio-pharmaceutical experience is a plus
+ Proven ability to communicate and present effectively to cross-functional and cross-organizational teams in a matrix environment
+ Strong leadership and analytical skills, ability to deliver on project objectives in a timely manner required
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
\#GD-SA
\#LI-SA
\#LI-Onsite
\#vhd
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video (************************************************** and check out our Diversity Equity and Inclusion actions at sanofi.com (************************************************************************ !
_US and Puerto Rico Residents Only_
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
_North America Applicants Only_
The salary range for this position is:
$133,500.00 - $192,833.33
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK (********************************************************************************************************* .
Global Terms & Conditions and Data Privacy Statement (***************************************************************
Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting ************** or via our movie We are Sanofi (*****************************
As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (************************************************
$133.5k-192.8k yearly 60d+ ago
Digital Product Lead - iCare Connect
Sanofi 4.3
Cambridge, MA jobs
Job Title: Digital Product Lead - iCare Connect
Grade: L3
About the Job
Ready to push the limits of what's possible? Join Sanofi in one of our corporate functions and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world.
At Sanofi, we're committed to providing the next-gen healthcare that patients and customers need. It's about harnessing data insights and leveraging AI responsibly to search deeper and solve sooner than ever before.
Sanofi (NYSE: SNY) is a leading global integrated healthcare company that discovers, develops, and distributes therapeutic solutions to improve the lives of everyone. The company works to prevent and treat the diseases of today, as well as those we may face tomorrow. With over 100,000 dedicated professionals in more than 100 countries, Sanofi is devoted to advancing healthcare around the world.
Sanofi is an equal opportunity employer that embraces diversity to foster positive, innovative thinking that will benefit people worldwide. Sanofi is also committed to employing qualified individuals with disabilities and, where warranted, will provide reasonable accommodation to applicants, as well as its employees.
Sanofi operates across multiple therapeutic areas including General Medicines, Specialty Care, Vaccines and Consumer Healthcare. The role of Digital ProductManager will focus on Sanofi's Specialty Care (externally known as Sanofi Genzyme). Specialty Care focuses on rare diseases, rare blood disorders, multiple sclerosis, oncology, and immunology. We help people with debilitating and complex conditions that are often difficult to diagnose and treat. Our approach is shaped by our experience developing highly specialized treatments and forging close relationships with physician and patient communities. We are dedicated to discovering and advancing new therapies, providing hope to patients and their families around the world. Learn more at **********************
The Global Digital Team for Specialty Care is focused on driving and accelerating digital transformation via delivery of digital products (marketing technology platforms, digital therapeutics, etc.) across the different therapeutic areas and directed at patients, physicians and/or payers. This team works to implement Sanofi's Digital strategy by bringing dedicated expertise internally at Sanofi and externally with digital health and/or technology partners to build the core digital foundation and drive growth thru digital across all business areas.
The Digital Product Owner, iCare is responsible for the successful design, build, and implementation of Sanofi's digital product line focused on patient support. Some of the products in the product line include, iCareConnect (Salesforce HealthCloud), iCareMarketing (Salesforce Marketing Cloud) and iCareEvents (Veeva Events Management). We have various therapeutic areas within Sanofi's specialty care division already live in the ecosystem while we are working on bringing a few other therapeutic areas on. In this role, the DPO will collaborate with the therapeutic area business leads and other digital product owners on the team to design, build, and implement a solution using Agile methodology. Strong collaboration and understanding across stakeholders will be critical to ensure iCare supports the needs of relevant cross-functional business partners in an efficient manner. The candidate must be solution-oriented, operationally savvy, creative, highly organized, flexible, and adept at working with multiple matrix teams, including external vendors.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
Responsible for helping with the product backlog with a goal to deliver on commitments on time, on budget and in line with business requirements
Collaborates with business product owners and iCare users to understand and document user flows and processes to ensure that the voice of the customer is incorporated into the product design
Works cross functionally across the digital organization specially with other digital product owners as well as customer experience team
Document and prioritize product specifications including goals, use cases, user stories, and business requirements
Continuously develops and communicates the value to the development teams and defines the features of the system
Contributes to the definition and maintains the Non-Functional Requirements (NFRs) to help ensure that the solution meets relevant standards and other system quality requirements
Manages the flow of work through the program Kanban and into the program backlog
Collaborates with other product owners for release management through the hypercare phase
Comfortable consulting with cross functional partners like legal, compliance, quality when needed
About You
Qualifications:
Bachelor's degree.
2-3 years of experience in business analysis; experience preferably on the patient services side preferred.
Demonstrated strong communication skills and customer service mindset
Completed training or certification in agile.
1 year of Salesforce experience
Preferences:
Experience with Marketing Cloud, Experience Cloud, Veeva Events
Demonstrated ability to work collaboratively as part of a matrix team
Proven ability to lead and influence teams without direct authority
Patient Support Services or other bio-pharmaceutical experience is a plus
Proven ability to communicate and present effectively to cross-functional and cross-organizational teams in a matrix environment
Strong leadership and analytical skills, ability to deliver on project objectives in a timely manner required
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA
#LI-SA
#LI-Onsite
#vhd
Pursue
progress
, discover
extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
US and Puerto Rico Residents Only
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
North America Applicants Only
The salary range for this position is:
$133,500.00 - $192,833.33
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.
$133.5k-192.8k yearly Auto-Apply 6d ago
CRM Product Lead (US Oncology)
Astrazeneca 4.6
Gaithersburg, MD jobs
Typical Accountabilities: • Leads development of brand strategy and marketing plans for assigned brand, which may include distribution channel solutions. • Participates in and evaluates market research and analyzes promotions, public relations, and advertising associated with assigned brands/products • Works closely with direct-to-consumer and managed markets teams to ensure successful positioning • Works closely with sales leaders to identify opportunities/issues • Participates in development of training for field/customer service personnel on brand information Typical People Management Responsibility (direct / indirect reports): • Approximate number of people managed in total (all levels) - What is the global remit? (how many countries will the role operate in?): Education, Qualifications, Skills and Experience: • Essential: Bachelor's Degree; Marketing and/or promotions experience; Experience developing a strategy and executing on that strategy; Experience managing complex projects; Understanding of the development and commercialization of pharmaceutical products in the US; Understanding of the US Healthcare environment • Desirable: MBA in relevant field; Experience in Consumer and/or Managed Markets strategy; Experience in Insight/Market Research; Sales and/or Sales Leadership experience; Experience in Emerging or DFL role Key Relationship to reach solutions: • Internal (to AZ or team): • External (to AZ):
Compensation Pay Range:
180,875.20 - 271,312.80 USD Annual
The annual base pay (or hourly rate of compensation) for this position is outlined above. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
06-Jan-2026
Closing Date
19-Jan-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.