Medical Director jobs at Bristol-Myers Squibb - 1503 jobs
Director, Clinical Site Operations
Bristol Myers Squibb 4.6
Medical director job at Bristol-Myers Squibb
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.
RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals
Summary
The Director, Clinical Site Operations provides strategic oversight, leadership and management of clinical trial execution, including oversight of site management and monitoring, consistent with RayzeBio corporate goals and program Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines and other applicable federal (FDA) and state regulations. The Director, Clinical Site Operations will also ensure that such operations activities are timely, efficient, and of the highest quality.
Job Responsibilities
Essential duties and responsibilities include the following. Other duties may be assigned.
Directs the operational oversight and execution of clinical site start-up, management and monitoring in accordance with RayzeBio SOPs, ICH Guidelines, and Good Clinical Practices (GCP) to ensure overall data quality, integrity, and patient protection and safety
Manages CRO relationship and oversight to ensure the appropriate scope of work, oversight and training of the clinical team, investigators and site staff as well as the achievement of study milestones within agreed upon timelines and budget
Develops collaborative relationships with investigative sites
Communicates clinical site performance data to the Head of Clinical Operations and the Clinical Program Management team
Key contributor to the development, review and approval of study documents including but not limited to RayzeBio SOPs and Clinical Operation Plans
Liaison with other functional departments to ensure that the highest quality is maintained
Participate in and/or lead departmental initiatives
Line management skills and expertise in mentoring and coaching
Detail oriented, organized and committed to quality and consistency
Excellent team-interaction skills and ability to work successfully in cross-functional teams
Ability to work in a dynamic environment with a high degree of flexibility
Represent RayzeBio at conferences as well as scientific and other business-related meetings as required
Assists in creating vision for department goals and objectives
Conduct oversight visits at investigational sites to ensure quality monitoring
Up to 20% travel required
Education and Experience
Minimum 10 years clinical operations experience within biotech, pharma or CRO industry
Proven experience in clinical research as team lead in clinical functions
BA/BS degree, scientific or healthcare discipline preferred
Skills and Qualifications
Independent professional who proactively communicates frequently and effectively.
Organized and able to work on multiple projects with tight deadlines.
High energy level; positive attitude; works well under stress; assertive and effective communicator.
Hands-on, action-oriented, and able to implement effectively.
Physical Demands
While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 15 pounds. Specific vision abilities required by this job include close vision and distance vision.
Work Environment
The noise level in the work environment is usually moderate.
#RayzeBio
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:
Remote - United States - US: $210,572 - $255,164
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.
R1598496 : Director, Clinical Site Operations
$210.6k-255.2k yearly Auto-Apply 2d ago
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US Medical Director - Neuromuscular and Neurodegenerative Diseases
Sanofi 4.3
Morristown, NJ jobs
The US MedicalDirector - Neuromuscular and Neurodegenerative Diseases leads medical strategy and thought leader engagement for Sanofi's neurology portfolio, including Riliprubart. This role involves cross-functional collaboration to support clinical development, product strategy, and medical education within the pharmaceutical industry. The position requires an MD, PhD, NP, or PharmD with expertise in neurology and experience in biologics or clinical care.
Job Title: US MedicalDirector - Neuromuscular and Neurodegenerative Diseases
Location: Cambridge, MA / Morristown, NJ
About the Job
Sanofi focuses on developing specialty treatments for debilitating diseases that are often difficult to diagnose and treat, providing hope to patients and their families. Learn
This leadership position reports to the Head of North America Neurology Medical, offering an opportunity to work in a patient-centric, high-performance culture. The role combines support for Sanofi's MS portfolio with primary responsibility for medical leadership of Riliprubart and other neurology pipeline assets in neuromuscular and neurodegenerative diseases.
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Main Responsibilities
Strategic Leadership
Lead US Neurology Medical activities related to Riliprubart and other pipeline assets addressing unmet needs in neuromuscular and neurodegenerative diseases
Develop and execute the annual US Medical Brand Plan aligned with critical success factors
Identify unmet medical needs in neuromuscular and neurodegenerative diseases addressable by Sanofi assets
Thought Leader Engagement
Cultivate relationships with current and future experts in MS, neuromuscular and neurodegenerative diseases across US academic and clinical medicine
Develop and implement KOL management plans with the cross-functional team
Gather expert insights to influence Clinical Development and Life Cycle Planning strategies
Product Strategy & Support
Collaborate with the cross-functional team to define and refine branded product strategy
Work with Clinical, Global Medical/Scientific Communications, Pharmacovigilance, and Statistics teams on post-hoc analyses and benefit/risk profile refinement
Support communication strategies for company-generated data in collaboration with Global Medical Scientific Communications
Cross-Functional Collaboration
Provide medical support, education, and guidance to Commercial, Marketing, Sales, and Market Access teams
Liaise with Global and US Neurology MedicalDirectors to ensure alignment across the organization
Participate in Medical Affairs, Clinical Sciences & Operations, and cross-functional teams and committees
About You
Qualifications
Education & Experience
MD, PhD, NP, or PharmD required
2+ years relevant experience in biologics/pharmaceutical industry OR relevant clinical experience.
Expertise in neuromuscular and neurodegenerative diseases, multiple sclerosis, and/or neurology preferred
Experience in both clinical development and patient care preferred
Professional Skills
Outstanding scientific acumen
Strong leadership and analytical skills with ability to deliver on project objectives
Proven ability to lead and influence teams without direct authority
Excellent communication, presentation, and organizational skills
Self-directed with ability to work independently with minimal direction
Collaborative and transparent leadership capabilities
Creative and innovative thinking
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
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Keywords:
MedicalDirector, Neuromuscular Diseases, Neurodegenerative Diseases, Pharmaceutical Industry, Clinical Development, Medical Leadership, Neurology, Product Strategy, Key Opinion Leader, Healthcare Management
$211k-300k yearly est. 2d ago
Associate Director Principal Medical Writer
Sanofi 4.3
Morristown, NJ jobs
The Associate Director Principal Medical Writer leads the creation and management of high-quality regulatory-compliant clinical documentation supporting drug development. This role involves implementing innovative digital technologies, managing cross-functional projects, and mentoring junior writers to ensure compliance and efficiency. The position requires deep expertise in clinical development processes, regulatory requirements, and document management systems.
Job Title: Principal Medical Writer Associate Director
Location: USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for attending occasional team meetings
About the Job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
Global Medical writing and Document management serves to generate timely, high quality, cost effective and regulatory compliant documents. Our mission is to synergize and harness evolving technologies pushing the edge of regulatory writing.
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:
Document Development
• Create high-quality regulatory-compliant clinical documents supporting product life cycle
• Ensure timely delivery while maintaining compliance with standards
Innovation
• Lead implementation of new digital technologies and AI solutions
• Drive process improvements for efficiency gains
Regulatory Expertise
• Prepare registration dossiers and Health Authority responses
• Monitor and implement regulatory documentation requirements
Project Management
• Lead cross-functional initiatives as Subject Matter Expert
• Drive change management within writing teams
Communication
• Update relevant stakeholders on project progress and needs
• Maintain accurate information in planning, tracking, and reporting tools Ensure consistent communication across ClinDoc functions
Coordination
• Mentor junior writers and review contract work
Quality & Training
• Develop training programs and documentation standards
• Build effective relationships with stakeholders and partners...
About You
Core Experience:
Six+ years as medical writer or equivalent specialist role
Proven track record leading multiple clinical documentation projects
Expert in clinical documentation preparation
Clinical Development Knowledge:
Demonstrated expertise in clinical development processes
Strong understanding of clinical study methodology and basic statistics
Knowledge of regulatory environment
Proficient in document management systems and authoring platforms
Professional Attributes:
Strong attention to detail and deadline management
Excellent organizational and follow-up abilities
Proven ability to work independently and in global teams
Technical skills:
• Expertise in electronic document management and Microsoft Office
• Proven experience in implementing emerging innovative digital technologies, including content reuse strategies and AI-assisted document authoring solutions.
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
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Keywords:
medical writer, clinical documentation, regulatory compliance, drug development, document management, clinical study methodology, regulatory writing, digital technologies, AI-assisted authoring, project management
$189k-297k yearly est. 2d ago
Associate Director, External Scientific Partnerships - US Medical Affairs
Alexion Pharmaceuticals, Inc. 4.6
Boston, MA jobs
Are you ready to make a difference in the world of rare diseases? As the Associate Director, External Scientific Partnerships, US Medical Affairs, you will be at the forefront of strategic initiatives with US-based health professional societies and associations. Collaborating with Director, ESP and TA Leadership teams, you will drive and deliver a comprehensive strategic engagement plan for our rare disease portfolio. Your role will involve professional society collaborations, HCP education, and engagement with Key Opinion Leaders, all aligned with US Medical Affairs' strategic goals. You will analyze and communicate key strategic external landscapes, enabling informed decisions that contribute to Alexion's success.
Accountabilities:
Maintain strategic relationships with US-based scientific societies and be responsible for execution of plans.
Align partnership initiatives with TA strategies and Leadership Teams to ensure evidence-based care and build the HCP talent pipeline.
Engage cross-functionally with Alexion leaders to optimize interactions related to scientific associations and identify collaboration opportunities.
Contribute to project objectives in line with medical strategy, incorporating new clinical evidence and guidelines.
Represent Alexion at key professional organization meetings and events, collaborating with internal collaborators.
Strategically fund programs through sponsorships, ensuring effective budget management.
Develop communications to ensure visibility of Alexion Professional Society partnerships.
Track and evaluate performance metrics to inform future strategy.
Undertake other strategic projects as assigned.
Essential Skills/Experience:
PhD, PharmD or equivalent experience in a scientific field preferred (BS, MS, MD, PhD, PharmD)
3-5 years of experience in the pharmaceutical field or alliance/partnership experience with large ESPOs and External Experts
Knowledge in rare disease and enterprise thinking; ability to tap into connections across products
Proven leadership and collaboration skills; shown capability in building relationships with diverse groups
Ability to foster strong, compliant, productive alliances
Proven ability to establish relationships with scientific associations and external experts
Ability to work in a highly matrixed environment; lead multiple projects and collaborate cross-functionally
Strong interpersonal, communication, and negotiation skills
Knowledge of drug development process and commercialization
Strong project management skills; track record in working effectively with cross-functional teams
Experience working in medical affairs
Fluent in English
Detailed knowledge of social media space, business channels, and advancing digital health
Solid understanding of regulatory environment and industry standards
Proven technical, organizational, project management, negotiation, and budgeting capabilities; self-starter
25% Travel anticipated
At AstraZeneca's Alexion division, we are driven by a passion for innovation and a commitment to making a meaningful impact. Our unique culture fosters connections that inspire new ideas, profoundly impacting patients' lives. We value diversity and inclusion, ensuring that life-changing ideas can emerge from anywhere. Our dedication to giving back to communities is matched by our ambition to succeed for those in need. Join us in a journey where your career is not just a path but an opportunity to make a difference where it truly counts.
The annual base pay for this position ranges from $150,202 - $225,304 USD Annual. 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 pay (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.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.
Ready to take the next step in your career? Apply now and be part of a team that is transforming lives every day!
Date Posted
21-Nov-2025
Closing Date
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.
$150.2k-225.3k yearly 2d ago
Medical Science Liaison CVRM - Baltimore, MD
Astrazeneca 4.6
Washington, DC jobs
At AstraZeneca, we turn ideas into life-changing medicines. Working here means being entrepreneurial, thinking big, and collaborating to make the impossible a reality. We focus on the power of science to address unmet patient needs worldwide. We commit to areas where we can truly change the course of medicine and bring ambitious new ideas to life.
As an Amyloidosis (ATTR) Medical Science Liaison (MSL), you'll play a pivotal role in channeling our scientific expertise to positively impact patient care.
About the BioPharmaceuticals Business Unit (BBU)
The BBU develops and drives therapeutic area and product strategies that address unmet patient needs globally. We integrate commercial, market access, medical, digital, and corporate functions to drive scientific innovation and commercial excellence in respiratory, cardiovascular, renal, and diabetes disease areas.
Why This Role Matters
As an ATTR MSL, you will be part of AstraZeneca's mission to transform clinical practice through science and technology. You'll partner with healthcare professionals to reduce acute episodes, disease complications, hospital admissions, and premature death. Through innovation, leadership, and sustainability, we put patients first.
What You'll Do
In this field-based role covering Baltimore, MD and surrounding areas, you will:
Engage in scientific discussions within priority accounts with healthcare professionals and researchers.
Collecting and sharing evidence-based insights.
Working within a cross functional environment to achieve positive impactful patient outcomes.
Build relationships with clinicians and researchers to support education and collaboration.
Find opportunities to improve patient outcomes and provide actionable insights to internal teams.
Respond to inquiries with clear, balanced scientific information about our products and disease areas.
Stay current on disease state management, emerging therapies, and the competitive landscape.
Deliver presentations and provide clinical support at regional and national meetings.
Ensure compliance with regulatory and company standards in all interactions.
Development Opportunities
Structured onboarding and continuous learning programs.
Exposure to clinical development activities and therapeutic brand strategies.
Opportunities to lead projects within the medical team and develop leadership skills over time.
Minimum Requirements
Advanced degree in a clinical or scientific field (MD, PharmD, PhD, NP, PA).
1-2 years of experience in clinical practice, research, or healthcare setting.
Understanding of business acumen such as healthcare delivery systems, payer structures, and treatment pathways.
Clinical experience in the relevant therapeutic area and ability to build professional relationships.
Strong communication skills to convey complex scientific information clearly.
Demonstrated ability to lead projects and influence cross‑functional teams.
Knowledge of regulatory and compliance requirements related to medical affairs.
Ability to travel 50-70% (varies by geography) including weekends and overnights.
Desirable Requirements
2+ years of pharmaceutical industry experience/ previous MSL.
Rare Disease and/or Cardiology.
Ability to build and leverage relationships to influence outcomes that improve patient care.
The annual base pay for this position ranges from US $147,363.20 to $233,698. Our positions offer eligibility for various incentives-an opportunity to receive short‑term incentive bonuses, equity‑based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted: 14-Jan-2026
Closing Date: 28-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.
#J-18808-Ljbffr
$147.4k-233.7k yearly 1d ago
Clinical Director
Jag Physical Therapy 4.2
Belleville, NJ jobs
The Physical Therapist Clinical Director is responsible for complete oversight of operations and administration of rehabilitative outpatient clinic providing Physical and Occupational Therapy. Ensures compliance with all regulations and health care requirements. This position is also responsible for patient evaluation and treatment.
Who We Are:
JAG Physical Therapy's care-first model of rehabilitation may be the change you are looking for! JAG Physical Therapy, a comprehensive outpatient, orthopedic physical therapy company with 100 facilities throughout Pennsylvania, New Jersey, and New York, is seeking compassionate and motivated individuals to join our winning team! JAG has been honored by the area's top publications as the best in the business based on growth and outcomes and is considered the Gold Standard for physical therapy care by the Metro area's largest healthcare systems and insurance providers.
What You'll Love About Us:
• up to $7,500 sign-on bonus
• up to $2,500 relocation bonus
• Competitive salary
• Yearly Bonus based on the performance of the Clinic
• Health, Dental, & Vision Benefits
• HSA Options including dependent care, medical, and commuter benefits
• $10,000.00 Term Life Insurance benefit at NO cost to employees
• up to 4 weeks PTO
• 401(k) with company match
• Continuing Education reimbursements
• MedBridge Membership
• Yearly review for growth opportunities
• Professional Development Growth Tracks
• Tuition discounts for employees and their families
• TicketsAtWork and LifeMart company perks
• Our workplace fosters a close-knit and supportive environment where individuals genuinely care for and uplift one another, creating a strong sense of unity and camaraderie
What You'll Need:
• Bachelors or Masters Degree required, Doctorate degree preferred
• Professional License/Certification required
• Valid CPR license
• Minimum of three years' clinical outpatient experience and two years' clinical supervision or clinical program development experience preferred
• Knowledge of EMR system
• Able to troubleshoot, keen sense for decision making and judgment; action oriented; approachable
• Team player and effective at building and fostering teamwork as well as maintain composure when dealing with conflict
• Excellent customer service skills, interpersonal and communication skills
What You'll Do:
• Responsible for meeting census goals of clinic and each clinician (office KPIs, number of patients seen). Scorecard review weekly with RCD
• Working with People Operations, ensures compliance with all federal and state employment laws.
• Facility maintenance
• Review and approve timecards through ADP ensuring adherence to all federal and state regulations with respect to Exempt and Non-Exempt staff
• Interview/hiring (clinical, admin, aide) in collaboration with HR- take out admin
• Training and onboarding clinical staff, ongoing evaluation of performance
• Resolve performance problems on a clinic level and elevating to HR when appropriate
• Monitor staff compliance
• Follow up with patients on low net promoter scores
• Monitor monthly budget of visits, labor, and clinical supplies
• Monitor documentation audits, Medicare compliance and patients approaching MMR cap
• Prompt EMR schedule review weekly
• Monitor staff unsigned notes
• Perform new patient eval audit weekly
• Manages and approves expenses of staff in clinic
• Physician referral management (outreach visits, Direct access review, etc)
• Clinical support staff expense management, scheduling, interviewing, hiring/termination
• Monitor discharge policy adherence
• Monthly clinical supply ordering
• Adhere to lost patient log workflow
• Weekly call with RCD
• Weekly meeting with OM
Important Disclaimer Notice:
The above statements are only intended to represent the essential job functions and general nature of the work being performed and are not exhaustive of the tasks that an Employee may be required to perform. The employer reserves the right to revise this at any time and to require Employees to perform other tasks as circumstances or conditions of its business, competitive considerations, or the work environment change. This job description is not a guarantee of employment. What you'll love about us section is based on full time employment with the company and is not guaranteed based on employment type.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
$69k-105k yearly est. 2d ago
CardioRenal Medical Science Liaison: Field Impact Leader
Astrazeneca 4.6
San Francisco, CA jobs
A global biopharmaceutical company seeks a Medical Science Liaison in San Francisco to support Cardiorenal marketed products. The role involves engaging with healthcare professionals, providing scientific support, and identifying patient management barriers. Candidates should have an advanced clinical degree and up to 2 years of experience in a clinical or commercial setting. Strong communication and leadership skills are essential. The position offers competitive pay and benefits.
#J-18808-Ljbffr
$145k-199k yearly est. 2d ago
ATTR Medical Science Liaison - Field-Based, Patient Impact
Astrazeneca 4.6
Washington, DC jobs
A leading biopharmaceutical company is seeking an Amyloidosis Medical Science Liaison (MSL) to engage with healthcare professionals and improve patient outcomes through scientific expertise. This role requires an advanced degree, clinical experience, and strong communication skills. The MSL will work in Baltimore, MD, focusing on reducing acute episodes and collaborating with cross-functional teams. The position offers competitive base pay with potential bonuses and comprehensive benefits.
#J-18808-Ljbffr
$130k-188k yearly est. 1d ago
Medical Science Liaison, CardioRenal - San Francisco, CA
Astrazeneca 4.6
San Francisco, CA jobs
At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life. As a Cardiovascular Renal (CVR) Medical Science Liaison, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives.
The BioPharmaceuticals Business Unit (BBU) creates and executes meaningful therapeutic area and product strategies that are focused on addressing the unmet needs of patients around the world. We are committed to changing the course of medicine and bringing innovative therapies to enhance the quality of life for our patients. The BBU integrates commercial, market access, medical, digital, and corporate functions to drive scientific development and commercial excellence in the core areas of respiratory, cardiovascular, renal and diabetes disease.
As a CVRM Medical Science Liaison you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. You will be a critical part of the evolution of how AstraZeneca is impacting practice change through innovative technological advances to include targeting high disease burden and low guideline based medical care. Our mission is to partner with health care practitioners to reduce acute episodes, disease complications, hospital admissions and premature death. Through science and innovation, growth and leadership with an emphasis on people and sustainability, we truly put patients first!
Typical Accountabilities
The CardioRenal Medical Science Liaison is a field-based professional with scientific, clinical and therapeutic area expertise responsible for providing medical and scientific support for Cardiorenal marketed products, new indications for current products, and compounds in development.
In this role, you will engage in scientific exchange with targeted Key Opinion Leaders (KOLs), Key Decision Makers (KDMs), and Healthcare Professionals (HCPs) consistent with the Medical Affairs organization's and Therapeutic Brand Teams' objectives.
Additionally, you will identify and engage key customers with scientific expertise and business knowledge of AstraZeneca marketed products and compounds in development. This includes developing peer-level relationships with Key Decision Makers (KDMs), HCPs and researchers consistent with Scientific and Medical Affairs strategy and objectives along with identifying pre-clinical, clinical and post-marketing study investigators in alignment with the goals of Clinical Development activities and Therapeutic Brand Teams initiatives.
As a Cardiorenal Medical Science Liaison, you will uncover barriers to optimal disease management, identify areas of greatest opportunity and readiness for improving patient outcomes, provide actionable information that enhances the value and appropriate use of company's products to internal stakeholders; respond to customer inquiries to ensure focused and balanced clinical and scientific information that supports the appropriate use of the company's products and services and deliver appropriate clinical and scientific information that clinically differentiates the company's products.
Additional accountabilities include adhering to internal standard processes and complying with regulatory and compliance requirements along with sustaining expertise in disease state management, emerging therapies and the competitive landscape; providing clinical support and delivering data presentations regionally and nationally; demonstrating project leadership and management in and across the field medical team and therapeutic area; training and mentoring within therapeutic area, providing performance guidelines and coaching.
Essential Requirements
Advanced Clinical/Science Degree required (e.g. MD, PharmD, PhD, NP, PA-C, etc. - BSN with extensive clinical experience may be considered)
0-2 years of experience in clinical or commercial setting
Thorough understanding of healthcare system landscape
Established networks and clinical experience within Therapeutic Area (TA) focus
Experience in pharmaceutical industry
Demonstrated expertise in discussing scientific content and context to multiple audiences
Excellent oral and written communication and interpersonal skills
Strong leadership capabilities
Excellent project management ability
Thorough knowledge of regulatory environment
Ability to travel 50-70% (percentage varies with geography)
Desirable Requirements
Established experience delivering quality improvement initiatives
2+ years' experience as a Medical Science Liaison in the pharmaceutical industry
Established track record of basic or clinical research
The annual base pay for this position ranges from US $147,363.20 & $233, 698. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
02-Jan-2026
Closing Date
15-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.
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$147.4k yearly 2d ago
Virology COVID MSL - Midwest Field Medical Liaison
Shionogi Inc. 4.4
Chicago, IL jobs
A leading pharmaceutical company is seeking a Medical Science Liaison in Chicago, Illinois. This role involves building relationships with healthcare professionals, responding to scientific inquiries, and collaborating across teams to meet medical objectives. Candidates should possess a doctoral degree in life sciences and previous MSL experience. The base salary range is $180,000-$210,000, with additional benefits included. The ideal candidate will reside in Chicago or surrounding suburbs.
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Cookie Notice* Identify, gain access to, and develop peer to peer relationships with regional and national thought leaders, active and potential study investigators, providers at academic and non-academic institutions and professional organizations within assigned geography.* Demonstrate and maintain deep scientific expertise on assigned Ipsen products and therapeutic area including competitive landscape and gaps in patient care.* Engage in ongoing scientific exchange about the science and clinical application of Ipsen's portfolio to external stakeholders to gather insights about current practice, treatment landscapes, and emerging data.* Assist with Company Sponsored Studies (CSS), including investigator/site identification, site initiation visits, education to support enrollment, and feedback regarding operational management to ensure optimal site selection and performance.* Partner with Medical Affairs and Medical Information services to ensure accurate delivery of medical and scientific information, as needed. Respond to on and off-label questions with integrity, compliance, and adherence to legal, regulatory, and Ipsen guidelines, policies & procedures.* Represent Ipsen and US Medical Affairs Team during scientific conferences, continuing medical educational events, and medical meetings.* Respond to unsolicited requests regarding interest in investigator sponsored studies (ISS) and supports ISS submissions, initiation and closure through appropriate internal processes, as needed.* Lead the development and implementation of a regional territory plan* Train and facilitate speakers on Ipsen's products.* Work efficiently and balance all work to enhance performance and execute local medical strategies within planned timelines.* Engage in continuous independent learning within the therapeutic area and actively attend and participate in upskilling programs related to Ipsen molecules, products, disease states and relevant business topics.* Differentiate Ipsen as the valued scientific partner of choice through innovative initiatives, coordinated strategy, scientific communication, and patient centricity.* Build and cultivate a close working relationship with all US cross-functional team members, including field-based counterparts and home office-based team members, marketing, HEOR, medical/clinical operations, etc. while maintaining full compliance with relevant company, industry, legal and regulatory requirements.* Support cross-functional teams to ensure operations are patient-focused, including rapidly responding to internal and external requests to discuss specific situations and challenges and provide medical affairs support to all stakeholders.* 2-3 years related MSL work experience required.* Previous Rare Disease experience required.* Knowledge of Rare Disease customer segments and market dynamics.* Excellent planning, presentation, written and presentation communication skills.* Demonstrated ability to develop and maintain credible and scientific relationships with top experts in the field.* Highly developed interpersonal skills and the ability to function on a cross-functional team.* Demonstrated expertise in ability to synthesize and communicate medical information clearly.* Knowledge of PhRMA, OIG, and other guidelines relating to compliant medical communications.* Knowledge of rare disease customer segments and market dynamics* Demonstrated expertise in discussing scientific content and context to multiple audiences.* Fundamental understanding of clinical research* Excellent project management ability* Excellent oral and written communication and interpersonal skills* Thorough knowledge of regulatory environment* Strong leadership capabilities* Excellent collaboration skills* Ability to travel (50-70%) based on size of geography.### Get In TouchIntroduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.
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$96k-168k yearly est. 3d ago
Medical Science Liaison, Rare Disease (New England)
Ipsen Group 4.9
Berkeley, CA jobs
Cookie NoticeMedical Science Liaison, Rare Disease (New England) page is loaded## Medical Science Liaison, Rare Disease (New England)locations: Berkeley Heightstime type: Full timeposted on: Posted Todayjob requisition id: R-20583**Title:**Medical Science Liaison, Rare Disease (New England)**Company:**Ipsen Biopharmaceuticals Inc.**About Ipsen:**Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company's success. Join us on our journey towards sustainable growth, creating real impact on patients and society!For more information, visit us at and follow our latest news on and .**Job Description:****WHAT -** **Summary & Purpose of the Position**The Medical Science Liaison (MSL) is a field-based scientific medical expert within Ipsen's U.S. Medical Affairs Rare Disease team. This role is responsible for engaging with national and regional Thought Leaders (TLs), Investigators, and Healthcare Providers (HCPs) to exchange scientific insights, support clinical research, and facilitate both clinical trial efforts and Investigator-Sponsored Studies (ISS).Leveraging deep clinical and scientific expertise, the MSL delivers non-promotional, evidence-based information on Ipsen's marketed and pipeline therapies. The MSL will play a key role in enhancing understanding of disease states, patient and physician journeys, Ipsen's products, and the broader competitive landscape to ultimately improve patient outcomes.The MSL will work closely with Ipsen colleagues across teams such as U.S. Medical Affairs, Clinical Development, and Commercial to ensure that scientific and technical needs are effectively identified and addressed.The MSL adheres to internal standard processes and complies with all regulatory and compliance requirements, while maintaining expertise in disease state management, emerging therapies, and the evolving treatment landscape.This is a field-based position covering the New England (MA, VT, NH, ME, CT, RI) through a mix of live (primary) and virtual channels. Eligible candidates must reside near a major airport within the territory.**WHAT -** **Main Responsibilities & Technical Competencies**Responsibilities will include, but are not limited to the following:* Identify, gain access to, and develop peer to peer relationships with regional and national thought leaders, active and potential study investigators, providers at academic and non-academic institutions and professional organizations within assigned geography.* Demonstrate and maintain deep scientific expertise on assigned Ipsen products and therapeutic area including competitive landscape and gaps in patient care.* Engage in ongoing scientific exchange about the science and clinical application of Ipsen's portfolio to external stakeholders to gather insights about current practice, treatment landscapes, and emerging data.* Assist with Company Sponsored Studies (CSS), including investigator/site identification, site initiation visits, education to support enrollment, and feedback regarding operational management to ensure optimal site selection and performance.* Partner with Medical Affairs and Medical Information services to ensure accurate delivery of medical and scientific information, as needed. Respond to on and off-label questions with integrity, compliance, and adherence to legal, regulatory, and Ipsen guidelines, policies & procedures.* Represent Ipsen and US Medical Affairs Team during scientific conferences, continuing medical educational events, and medical meetings.* Respond to unsolicited requests regarding interest in investigator sponsored studies (ISS) and supports ISS submissions, initiation and closure through appropriate internal processes, as needed.* Lead the development and implementation of a regional territory plan* Train and facilitate speakers on Ipsen's products.* Work efficiently and balance all work to enhance performance and execute local medical strategies within planned timelines.* Engage in continuous independent learning within the therapeutic area and actively attend and participate in upskilling programs related to Ipsen molecules, products, disease states and relevant business topics.* Differentiate Ipsen as the valued scientific partner of choice through innovative initiatives, coordinated strategy, scientific communication, and patient centricity.* Build and cultivate a close working relationship with all US cross-functional team members, including field-based counterparts and home office-based team members, marketing, HEOR, medical/clinical operations, etc. while maintaining full compliance with relevant company, industry, legal and regulatory requirements.* Support cross-functional teams to ensure operations are patient-focused, including rapidly responding to internal and external requests to discuss specific situations and challenges and provide medical affairs support to all stakeholders.**HOW - Knowledge & Experience**Knowledge & Experience (essential):* 2-3 years related MSL work experience required.* Previous Rare Disease experience required.* Knowledge of Rare Disease customer segments and market dynamics.* Excellent planning, presentation, written and presentation communication skills.* Demonstrated ability to develop and maintain credible and scientific relationships with top experts in the field.* Highly developed interpersonal skills and the ability to function on a cross-functional team.* Demonstrated expertise in ability to synthesize and communicate medical information clearly.* Knowledge of PhRMA, OIG, and other guidelines relating to compliant medical communications.* Knowledge of rare disease customer segments and market dynamics* Demonstrated expertise in discussing scientific content and context to multiple audiences.* Fundamental understanding of clinical research* Excellent project management ability* Excellent oral and written communication and interpersonal skills* Thorough knowledge of regulatory environment* Strong leadership capabilities* Excellent collaboration skills* Ability to travel (50-70%) based on size of geography.Knowledge & Experience (preferred):* Previous experience with product launches and life cycle management strongly preferred.Education / Certifications (essential):* Doctoral level in the sciences required (MD, DO, PhD, PharmD, Nursing or equivalent).Language(s) (essential):* Fluent in English.Ipsen Biopharmaceuticals, Inc. is an equal opportunity employer. We recruit, employ, train, compensate, and promote without regard to race, religion, creed, national origin, age, gender, sexual orientation, sexual identity, marital status, military or veteran status, disability, genetic information, or any other category protected by applicable federal, state or local law.Ipsen Biopharmaceuticals, Inc. conducts background screening, reference checks, and drug testing as part of its pre-employment screening process. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned.All Employees are expected to adhere to all company policies and act
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$96k-168k yearly est. 5d ago
Senior Medical Science Liaison - Nephrology (Michigan: East)
Vertex Pharmaceuticals 4.6
Boston, MA jobs
Senior Medical Science Liaison - Nephrology (Michigan: East) page is loaded## Senior Medical Science Liaison - Nephrology (Michigan: East)locations: Boston, MAtime type: Full timeposted on: Posted Todayjob requisition id: REQ-26679**Job Description****General Summary:**The Senior Medical Science Liaison (Sr MSL) (Nephrology) for Povetacicept programs. Povetacicept (pove) is an enhanced, dual BAFF/APRIL inhibitor in pivotal development for the treatment of IgA Nephropathy (IgAN).The Sr MSL will serve as a scientific liaison to the medical/academic community and is responsible for establishing and maintaining relationships with Health Care Providers/Professionals (HCPs) to ensure the appropriate dissemination of clinical and scientific information regarding Vertex' compounds in a timely, ethical and stakeholder-focused manner. The Sr MSL will contribute to shaping the medical plan by providing external stakeholders' insights and contribute to the designing and execution of the Medical Affairs strategy and plan. The Sr MSL will engage HCPs in response to scientific educational and research needs with available Vertex resources and provide the latest emerging data in response to specific inquiries, as appropriate.**Key Duties and Responsibilities:*** Develops and fosters effective and trusting relationships with Thought Leaders (TL) and identifies and engages other appropriate HCPs resulting in scientific engagement with a large network of T1D and transplant-team care providers and opinion leaders. Additionally, understands the inter-relationships both within and between academic centers and utilizes this expertise to enhance Thought Leader and HCP engagements* Consistently incorporates all aspects of the SEM (Scientific Engagement Model) into all interactions, enhancing the quality of interactions and overall relationships as assessed by field coaching observations* Independently incorporates the medical plan into interactions and territory planning (i.e. listening priorities) and captures valuable feedback in the CRM system to inform internal stakeholders and assist in shaping the medical strategy* Possesses an in-depth understanding of the utility and functionality of the CRM system/data analytics tools, allowing for the time sensitive capture of interaction details. Uses CRM/Analytics to enhance future TL engagements and manage workload* Discusses scientific information effectively and compliantly with external stakeholders at an advanced level of communication for both disease state and product to external stakeholders as assessed by management coaching and field observations* In-depth conceptual and practical knowledge of payers in the region and possesses an in-depth understanding of the impact of payers on patient care delivery* Assists clinical development/clinical operations by fully understanding IB content and presenting IB material, providing nominations for trial sites as requested, providing end of study data reviews with investigators (as needed)* Represents Vertex at medical congresses by providing scientific session/abstract coverage, booth staffing coverage, routine TL interactions, contributing to the daily and end of congress summaries and may provide logistical guidance through organizing and scheduling abstract/session coverage and preparing and delivering the conference debrief (as needed)* May serve as a mentor or trainer for colleagues with less experience; for example, assisting with new hire MSL onboarding* Conducts all activities in compliance with Vertex policy and procedures and performs all administrative tasks in a timely manner such as CRM entry, vehicle mileage reporting, expense reporting, calendar entries, training assignments, etc.**Knowledge and Skills:*** Ability to complete goals within allotted timeframes, and deliver high quality results* Ability to help plan and complete projects in a constantly changing field-based environment* Ability to appraise and comprehend medical and scientific literature* Ability to effectively present clinical/scientific information in a credible manner in varied settings* Good knowledge of assigned geographic territory* In-depth understanding of healthcare regulatory environment* Apply proficient knowledge of relevant T1D and T1D management protocols, healthcare environment and landscape to articulate the medical and scientific value of our products* Demonstrated working understanding around the compliance and regulatory frameworks that govern the pharmaceutical industry and conducts compliant interactions with internal and external stakeholders.* In-depth knowledge of payers and unique medical information needs to support access and appropriate use of Vertex medicines* Good knowledge of Health Economics and Outcomes Research* Fluent in English (oral and written)**Education and Experience:*** Minimum requirement for advanced biomedical or life sciences degree (ex. Masters, NP, PA)* Requires minimum of 3-4 years of experience as an MSL supporting Nephrology programs or in other medical affairs roles in the pharma/biotech industry or the equivalent combination of education and experience.* Previous training or experience in designated therapeutic area is helpful Pay Range:$171,300 - $245,000Disclosure Statement:The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.**Company Information**Vertex is a global biotechnology company that invests in scientific innovation.Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com.
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$171.3k-245k yearly 4d ago
Field Medical Science Liaison - Cancer Diagnostics
Upsher-Smith 4.7
Palo Alto, CA jobs
A leading diagnostics company seeks a Medical Science Liaison to provide clinical education to healthcare professionals and support internal teams. The role requires strong communication skills, clinical expertise, and at least 5 years of experience, preferably in urology. Candidates located in major cities in the United States are preferred. The MSL will travel approximately 60% of the time and engage in significant educational initiatives. Competitive compensation and inclusive workplace offered.
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$130k-220k yearly est. 4d ago
Director of Trauma & ECC: Lead Care & Improvement
Academy of Managed Care Pharmacy 3.4
Tyler, TX jobs
A healthcare organization is seeking a Director of Trauma in Tyler, Texas. The ideal candidate is a registered nurse with leadership experience in trauma care, holds a Master's degree, and has strong communication skills. Responsibilities include program oversight, educational opportunities for staff, and liaising with administration for quality trauma care. This full-time position requires active participation in budget processes and performance improvement initiatives.
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$50k-76k yearly est. 2d ago
Senior Medical Science Liaison - Nephrology (Missouri/Iowa/Nebraska/ Illinois:...
Upsher-Smith 4.7
San Rafael, CA jobs
Senior Medical Science Liaison (Sr MSL) (Nephrology) for Povetacicept programs. Povetacicept (pove) is an enhanced, dual BAFF/APRIL inhibitor in pivotal development for the treatment of IgA Nephropathy (IgAN).
The Sr MSL will serve as a scientific liaison to the medical/academic community and is responsible for establishing and maintaining relationships with Health Care Providers/Professionals (HCPs) to ensure the appropriate dissemination of clinical and scientific information regarding Vertex' compounds in a timely, ethical and stakeholder-focused manner. The Sr MSL will contribute to shaping the medical plan by providing external stakeholders' insights and contribute to the designing and execution of the Medical Affairs strategy and plan. The Sr MSL will engage HCPs in response to scientific educational and research needs with available Vertex resources and provide the latest emerging data in response to specific inquiries, as appropriate.
Key Duties and Responsibilities
Develops and fosters effective and trusting relationships with Thought Leaders (TL) and identifies and engages other appropriate HCPs resulting in scientific engagement with a large network of T1D and transplant-team care providers and opinion leaders. Additionally, understands the inter-relationships both within and between academic centers and utilizes this expertise to enhance Thought Leader and HCP engagements
Consistently incorporates all aspects of the SEM (Scientific Engagement Model) into all interactions, enhancing the quality of interactions and overall relationships as assessed by field coaching observations
Independently incorporates the medical plan into interactions and territory planning (i.e. listening priorities) and captures valuable feedback in the CRM system to inform internal stakeholders and assist in shaping the medical strategy
Possesses an in-depth understanding of the utility and functionality of the CRM system/data analytics tools, allowing for the time sensitive capture of interaction details. Uses CRM/Analytics to enhance future TL engagements and manage workload
Discusses scientific information effectively and compliantly with external stakeholders at an advanced level of communication for both disease state and product to external stakeholders as assessed by management coaching and field observations
In-depth conceptual and practical knowledge of payers in the region and possesses an in-depth understanding of the impact of payers on patient care delivery
Assists clinical development/clinical operations by fully understanding IB content and presenting IB material, providing nominations for trial sites as requested, providing end of study data reviews with investigators (as needed)
Represents Vertex at medical congresses by providing scientific session/abstract coverage, booth staffing coverage, routine TL interactions, contributing to the daily and end of congress summaries and may provide logistical guidance through organizing and scheduling abstract/session coverage and preparing and delivering the conference debrief (as needed)
May serve as a mentor or trainer for colleagues with less experience; for example, assisting with new hire MSL onboarding
Conducts all activities in compliance with Vertex policy and procedures and performs all administrative tasks in a timely manner such as CRM entry, vehicle mileage reporting, expense reporting, calendar entries, training assignments, etc.
Knowledge and Skills
Ability to complete goals within allotted timeframes, and deliver high quality results
Ability to help plan and complete projects in a constantly changing field-based environment
Ability to appraise and comprehend medical and scientific literature
Ability to effectively present clinical/scientific information in a credible manner in varied settings
Good knowledge of assigned geographic territory
In-depth understanding of healthcare regulatory environment
Apply proficient knowledge of relevant T1D and T1D management protocols, healthcare environment and landscape to articulate the medical and scientific value of our products
Demonstrated working understanding around the compliance and regulatory frameworks that govern the pharmaceutical industry and conducts compliant interactions with internal and external stakeholders.
In-depth knowledge of payers and unique medical information needs to support access and appropriate use of Vertex medicines
Good knowledge of Health Economics and Outcomes Research
Fluent in English (oral and written)
Education and Experience
Minimum requirement for advanced biomedical or life sciences degree (ex. Masters, NP, PA)
Requires minimum of 3-4 years of experience as an MSL supporting Nephrology programs or in other medical affairs roles in the pharma/biotech industry or the equivalent combination of education and experience.
Previous training or experience in designated therapeutic area is helpful
Pay Range
$171,300 - $245,000
Disclosure Statement
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com.
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$171.3k-245k yearly 4d ago
Senior Nephrology MSL - Strategic Medical Liaison
Upsher-Smith 4.7
San Rafael, CA jobs
A leading biotechnology firm located in California is seeking a Senior Medical Science Liaison for Nephrology programs. This role requires developing scientific relationships with healthcare professionals, effectively communicating clinical information, and supporting the company's medical affairs strategy. Ideal candidates will possess an advanced degree in biomedical sciences and a minimum of 3-4 years of experience in medical science liaison roles related to nephrology. Competitive salary range from $171,300 to $245,000, with various employee benefits.
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$171.3k-245k yearly 4d ago
Medical Science Liaison
Upsher-Smith 4.7
Palo Alto, CA jobs
At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way: it's about how we work together, guided by our values, to give clinicians the insights they need to help patients make life‑changing decisions.
Our Values:
We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care
We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work
We Are Stronger Together: We collaborate openly, seek to understand, and celebrate our wins
We Care Deeply: We embrace our differences, do the right thing, and encourage each other
The Position:
Our Medical Science Liaisons (MSLs) are a critical part of the Decipher Urologic Cancers business group. They are clinical/genomic experts who provide clinical product education to our customers and our field teams with the goal of driving understanding and adoption of our novel diagnostics. Our MSLs have strong communication skills and are energized by building rapport with our HCP customers as well as our sales team and addressing their educational and customer needs. They will be expected to partner closely across the organization to serve as a scientific and clinical resource for the company's products and associated disease states, providing both internal and external educational support. This also includes providing support for the development of multi‑channel medical educational activities and tools across the product lifecycle such as speaker programs, educational materials, slide creation, and online educational events.
The MSL functions as a field‑based member of the marketing department within the commercial team. This is a full‑time position with approximately 70% of the time devoted to client‑facing activities mostly at the request of the sales team, in‑person and remote, and 30% spent on internal collaborations and special projects.
This role requires at least 60% travel and provides coverage of key customers and support of field teams over multiple states in the United States. The coverage geography will be spread amongst states in the Midwest and Northwest, with occasional trips to other parts of the country.
We prefer candidates located in San Diego, Denver, Dallas, Seattle, St. Louis and Kansas City.
Who You Are:
Advanced scientific or clinical degree required - PhD, MD, NP, PA, CGC
At least 5 years of clinical experience preferably urology/radiation oncology‑focused
Prior experience as an MSL in the introduction of a novel clinical assay preferred
Advanced understanding of tumor biology and molecular testing and/or related working experience critical for success in this role
Outstanding interpersonal skills and a team player, demonstrating customer centricity, passion for patients and desire to help the cross‑functional teams succeed
Outstanding oral and written presentation skills, to convey complex study findings and data to audiences with varying degrees of scientific/clinical/healthcare knowledge
Outstanding interpersonal skills in building rapport, probing, situational awareness and adapting communication and content based on real‑time needs of audience
Willingness and ability to travel within defined region with proximity to a major airport
A detail‑oriented, organized, self‑starter approach, with strong ability to multitask yet prioritize workload
Pay range $165,000-$192,000 USD
What We Can Offer You
Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient‑oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.
About Veracyte
Veracyte (Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high‑value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high‑performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence‑generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit **************** or follow us on LinkedIn or X (Twitter).
Veracyte, Inc. 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 or disability status. Veracyte participates in E-Verify in the United States. View our CCPA Disclosure Notice.
If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to ********************
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$165k-192k yearly 4d ago
Medical Science Liaison / Senior Medical Science Liaison (Midwest)
Verastem Oncology 3.7
Chicago, IL jobs
Company Profile:
At Verastem Oncology, we're advancing innovation and addressing the urgent needs of patients living with cancers driven by RAS/MAPK pathway mutations, a key driver of tumor growth and treatment resistance. The FDA approval of AVMAPKI FAKZYNJA CO-PACK delivered the first therapy specifically for women living with recurrent KRAS-mutated low-grade serous ovarian cancer, a rare cancer with significant unmet need. We've successfully launched this innovative combination therapygate in the U.S. and are exploring regulatory pathways for Europe and Japan.
We are continuing to advance our pipeline of drugs that we believe will help block cancer cell survival, inhibit tumor growth, and overcome treatment resistance. With clinical trials underway, we have an exciting opportunity to shape the future of cancer care and make a meaningful impact in the lives of patients.
Summary
The Medical Science Liaison (MSL) role is the field-based medical/scientific expert for Verastem Oncology, focusing on engagement with healthcare providers to provide fair/balanced education on Doc investigational products, understanding the evolving therapeutic landscape, and supporting research collaborations across the portfolio.
Territory includes IL, MN, MO, IA, ND, SD, NE, and WI. Preferred locations for candidates to reside include Chicago, Minneapolis, and St. Louis.
Roles and Responsibilities< strangely> MSL:
Identifies, establishes, and maintains collaborative relationships with key investigators, institutions, groups and consortia in disease state areas of strategic focus forandung company.
Provides education to the medical community on company's investigational products and disease areas of focus.
Increases company visibility and enhances professional interaction with current and future oncology leaders.
Participates in medical education for healthcare professionals, including formulary (P&T) committees, through presentations at appropriate venues.
Works with the appropriate departments/personnel at clinical sites to ensure required education and training are होटल provided Completable.
Identifies clinical research opportunities that are consistent with company objectives.
Is the primary territory contact for the investigator-initiated research program, facilitating the processheiro concept submission through publication.
Identifies and communicates key clinical and research insights from oncology leaders to help shape company research.
Maintains a high level of clinical and scientific expertise through ongoing training and self-education, including attendance of relevant conferences, scientific workshops, and review of key publications.
Gathers and disseminates competitive intelligence in a compliant manner.
Takes advantage of opportunities to mentor other MSL team members, and actively contributes to cross-functional Medical Affairs team.
(language) Effectively executes administrative aspects of regional field activities.
Substantively contributes to, and provides medical leadership for internal cross functional programs/projects.
Provides responses to unsolicited requests for medical information, often in direct collaboration with Medical Information Services personnel.
Completes accurate and timely reports, project plans, and required documentation requests.
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Senior MSL:
The senior MSL will have all the responsibilities of an MSL and will have also consistently demonstrated core competencies and will assume broader responsibilities, that may include one or more of the following.
Substantively contributes to scientific publication planning, slide-deck development, training initiatives and the development/implementation of a Medical Strategy Plan.
Leading national level priority projects or cross-functional initiatives on behalf of Medical Affairs.
Leading interactions for specific select priority projects with external collaborators or groups.
Mentoring or coaching responsibilities for other MSLs especially new hires.
Coordinating with MA Training for identifying.constraints delivering advanced training initiatives
Experience, Education and Specialized Knowledge and Skills MSL:
Advanced Clinical/Science degree (MSN, PharmD, PhD) or professional credentials/ equivalent required with prior experience in the biotech/pharmaceutical industry, strongly preferred.
Prior MSL or relevant experience is strongly preferred.
Minimum of 3 years oncology experience, especially in gynecologic oncology, is strongly preferred.
Knowledge of applicable treatment, compliance, and regulatory guidelines.
Excellent interpersonal communication and presentation skills.
Strong problem solving, decision-making, and negotiation skills.
Ability to think strategically and apply knowledge and analytical skills.
Ability to summarize complex scientific information and present in a clear, concise, confident, and scientifically accurate and balanced manner to a range of audiences.
Ability to network and partner with external customers, including medical thought leaders, academic institutions, research consortia, and practice networks.
Thrives in a team environment and enjoys cross-functional collaboration; positively contributes to team culture.
Possesses demonstrable effective leadership skills (by example and through accomplishments) and can step forward to handle challenges within scope of authority.
Demonstrates deep therapeutic competency; stays abreast of trends and new information in the therapeutic/translational science area, as well as the profession at large.
Senior MSL:
For Senior MSL must meet the qualifications for MSL with a minimum five (5) years in Pharmaceutical Industry Medical Affairs as MSL, candidates with solid tumor experience preferred.
Ability to travel up to 65% of the time: As this is a customer-facing position, and the geographic territory expected to!!!!!/{
Knowledge of treatment guidelines (NCCN, ASCO, ESMO, etc.), clinical research processes, FDA regulations, CMS reimbursement coverage process, and OIG guidelines.败段>
Knowledge or experience in ovarian cancer/gynecologic oncology is a plus.
Must have the ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, NCI Cooperative Group leadership and members, medicaldirectors of medical groups or insurance carriers, as well as pharmacy directors.
Must be highly articulate and self-confident during formal and informal presentations; able to convey complex, scientific ideas fluently to any audience.
Travel:
Approximately 60-70% domestic travel is required.
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$88k-165k yearly est. 4d ago
Senior Oncology Medical Science Liaison - Field Leader
Verastem Oncology 3.7
Chicago, IL jobs
A leading oncology company is seeking a Medical Science Liaison (MSL) to engage with healthcare providers, providing education on investigational products and supporting research collaborations across multiple states. Candidates should have an advanced clinical degree, oncology experience, and excellent communication skills. This role requires significant travel across Illinois and surrounding areas to maintain key relationships and educate medical professionals. Join us in advancing cancer treatment innovations.
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