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Senior Director jobs at Gilead Sciences - 402 jobs

  • Sr. Director R&D E-Systems & AI Quality

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    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. POSITION OVERVIEW Would you like to play a crucial role in developing life‑saving therapies? Are you excited to use your scientific insight to partner with internal teams, and external partners as we strive to cure unmet medical needs? The Central Quality team within R&D Quality (RDQ) is seeking a seasoned leader to activate Electronic Systems and Artificial Intelligence Quality for the Development organization. In this role you will focus on two critical areas for the business: (1) defining and executing the R&D Quality Digital & Controls Strategy inclusive of understanding the implications of digital tools such as Artificial Intelligence (AI), Machine Learning (ML), Robotic Process Automation (RPA) and other digital tools; and (2) building partnerships across Development, IT and other functions and elevating Quality as a trusted advisor. The ideal candidate will have a strong point of view and be able to effectively influence stakeholders cross‑functionally with proven experience in modernizing Quality & Compliance practices, standards and approaches to novel technologies. KEY RESPONSIBILITIES Define and execute the Quality strategy for Development Electronic Systems including the use of Artificial Intelligence (AI), establishing clear standards, goals, and a long‑term roadmap that ensures compliance, data integrity, and business enablement. Enable the adoption of emerging technologies (e.g. RPA, AI, ML, LLMs) by embedding fit‑for‑purpose quality controls into processes, ensuring Quality serves as a driver of innovation rather than a barrier and that digital solutions enable compliance, efficiency, and innovation. Champion the use of automation and digital solutions to enable CSV / CSA activities and increase transparency. Drive a risk‑based approach to validation and eSystem related data integrity. Partner with IT and Business functions to modernize E‑Systems Quality and maintain alignment with the evolving regulatory landscape. Champion unification of Electronic Systems policies and procedures across PDM, Commercial, and IT. Lead and facilitate change management strategy and activities related to strategy and process change. OPERATIONAL EXCELLENCE AND OVERSIGHT Oversee Development systems and applications, as well as the use and applicability of emerging technologies such as AI and ML for Development. Engage and advise in cross‑functional governance to ensure Quality is a key consideration in technology initiatives, serving as a trusted advisor to IT and business stakeholders. Advise and support the R&D Data Governance Council with a focus on Data Integrity, Privacy and Protection. Serve as Development Global Process Owner for E‑systems Quality incl. process, issues, risks, inspection and audit requests. Identify and implement process improvements to enhance output and efficiency of E‑System compliance. Define and implement meaningful metrics to measure E‑Systems Quality performance, increasing transparency, driving accountability. Oversee the execution of Development QA activities, including testing, validation, and risk management ensuring alignment with modern CSA principles. Ensures compliance with data privacy and security regulations and maintain a high level of data integrity. Anticipate and mitigate risks across the Development E‑Systems portfolio, proactively resolving delivery roadblocks and aligning stakeholders. Utilize data‑driven insights to perform trend analysis on CAPAs, deviations, and other quality events, identifying systemic issues as well as actionable strategies that enhance compliance, operational efficiency, and proactive risk management. Ensure Development E‑Systems maintain continuous audit readiness, while leading efficient audit execution support through coordinated responses and effective stakeholder engagement. Manage vendor relationships and ensure cost‑effective, value‑aligned execution across strategic initiatives. Drive accountability for maintaining SaaS vendor‑managed eSystems in a validated and compliant state, ensuring alignment with data integrity (DI) standards. Shaping enterprise‑level strategies that mitigate risk, strengthen regulatory readiness, and enhance data governance and system resilience across the digital ecosystem. COMPETENCIES Clearly understands the value and challenges with adoption of digital tools including AI, ML, RPA. Innovation Enablement - Forward‑looking mindset with the ability to embrace and integrate emerging technologies (e.g. AI/ML, cloud, and automation) into regulated environments. Lead, influence and unify various stakeholders with different backgrounds, strengths, and abilities to create high‑functioning teams. Cross‑Functional Collaboration - Skilled at building partnerships across IT, R&D, Manufacturing, and Commercial functions; trusted advisor and influencer. Change Leadership - Proven ability to lead cultural and organizational change. Risk‑Based Thinking - Expertise in applying risk management principles to simplify processes (e.g., CSA over CSV) while maintaining compliance. Continuous Improvement - Lean mindset with experience streamlining processes, harmonizing SOPs, and reducing silos. Excellent communication skills, active listener. Demonstrated complex problem‑solving skills and creative solution development and ongoing issue resolution. Ability to make effective, defensible business decisions in the best interest of Gilead and the project / program. Recruit, manage and provide leadership and guidance to Quality Learning and Development staff/team members. Lead, mentor and coach project team and junior team members. REQUIREMENTS Deep understanding of R&D / Development system / application quality assurance methodologies, testing techniques and risk management. Strong familiarity with relevant R&D electronic systems regulations and standards, including GxP regulations in the biopharmaceutical industry. Proven ability to lead and motivate a team, provide guidance, and drive change. Ability to identify and resolve complex quality and compliance issues. Good understanding of and experience with change management principles. Bachelor of Science or Arts degree, advanced degree preferred. 13+ years of pharmaceutical industry - IT and / or Development. Demonstrated excellence in written and oral communication. Experience managing and overseeing external vendors. Ability to develop and manage a budget. Significant experience working with and establishing strong relationships across R&D functions. Applied knowledge of performance measurements (e.g., metrics, dashboards). Proven ability to delegate in matrix environment, predict issues, anticipate risks and solve problems. Strong leadership presence with demonstrated ability to lead without authority and influence programs, projects and/or initiatives. Strong EQ soft and interpersonal skills and with proven understanding of team dynamics. Strong negotiation and conflict resolution skills. Ability to recognize and make hard decisions that directly impact staff. When needed, ability to travel. 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*. * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Equal Employment Opportunity Statement 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 any other non‑job related characteristic 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. Gilead Sciences will not discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. Employees who have access to the compensation information of other employees or applicants as part of their essential job functions cannot disclose the pay of others to individuals who do not otherwise have access to that information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing or action, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. For Current Gilead Employees and Contractors Please apply via the internal career opportunities portal in Workday. Job Requisition Information Job Requisition ID: R0049072 Full Time / Part Time: Full‑Time Job Level: Director Remote Type: Onsite Required #J-18808-Ljbffr
    $243.1k-314.6k yearly 2d ago
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  • Senior Director, Global Distribution QA

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    A leading biopharmaceutical company in California is seeking a Senior Director of Quality Assurance - Distribution. This role involves leadership in QA processes within a diverse distribution network, requiring over 14 years of experience in the field. The ideal candidate will drive performance and compliance while collaborating with key stakeholders. The salary range is $243,100 - $314,600 annually, with additional benefits. #J-18808-Ljbffr
    $243.1k-314.6k yearly 5d ago
  • Senior Director, Strategic Market Access & Execution

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    A major biopharmaceutical company located in California seeks a Senior Director for Strategic Market Access Initiatives. This role involves leading initiatives, developing strategies in market access, and representing senior leadership in strategic discussions. Candidates should have significant experience in pharmaceutical market access and demonstrate exceptional leadership capabilities. The position offers a competitive salary range of $243,100 - $314,600 with additional benefits. #J-18808-Ljbffr
    $243.1k-314.6k yearly 4d ago
  • Senior Director, Global Supplier Quality

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    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. Senior Director, Global Supplier Quality Gilead Sciences, Inc. is a research‑based biopharmaceutical company founded in 1987. Together we deliver life‑saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Working in PDM Global Quality at Gilead Pharmaceutical Development & Manufacturing (PDM) Global Quality delivers on Gilead's commitment to bring life‑changing therapies to patients through robust Quality processes and systems. Our approach is agile, innovative and collaborative and our teams are committed to the successful delivery of safe life‑changing therapies. Job Summary Lead a team of 10-15 Quality Professionals to define, lead and manage the Global Supplier Quality program by providing quality oversight of GMP material and commodity suppliers. Work collaboratively with internal and external networks to continually improve Gilead's Global Supplier Quality program, including selection, onboarding, qualification and routine quality and performance oversight of global and local GMP material and commodity suppliers. Demonstrate leadership skills, extensive working knowledge of managing GMP material and commodity suppliers' performance and relationships, and exceptional skills in managing a matrix organization. Understand different material categories supporting GMP manufacturing of different Gilead product modalities. Influence Gilead's external network on selection of GMP material and commodity suppliers in alignment with Gilead's standards. Be extremely familiar with applicable regulations and requirements in GMP material and commodity supplier management, and clarify the role and responsibilities between marketing authorization holder and contract manufacturing organizations. Possess strong communication, influencing and negotiation skills; evaluate options and trade‑offs and utilize available resources to achieve the most positive impact to the business; partner with leaders in different PDM functions including Technical Development, Packaging Development and Engineering, Global Manufacturing, Procurement, Regulatory CMC, and the Gilead Site Quality. Have proven track record in leading Global Supplier Quality program in other global biotech or pharmaceutical companies, preferably with established relationships with reputable GMP material and commodity suppliers. Job Functions Execute an integrated and sustainable Global Supplier Quality strategy for Gilead's clinical and commercial products, based on the value proposition for Gilead (Integrity, Inclusion, Teamwork, Accountability, Excellence) and available SMEs. Develop processes to communicate learnings and drive related Supplier Quality improvement initiatives. Develop a process for exchange of lessons learned across multiple company representatives and identify opportunities for process improvements. Collaborate with Technical and Quality leadership to identify solutions and processes and align with key partners on implementation of new requirements. Implement continuous improvement initiatives to drive Global Supplier Quality program and ensure maximum productivity and world‑class systems, meeting the needs of all internal and external constituencies with emphasis on process, quality, productivity, budget control, and profitability. Develop, implement, and monitor Global Supplier Quality program, policies, and procedures to ensure compliance with GxP standards, corporate policies, FDA, EMA, and other regulatory body regulations and guidelines. Set and drive compliance with department, site and global KPIs. Evaluate current Global Supplier Quality systems and processes and recommend and implement appropriate enhancements and training to achieve Gilead's long‑term objectives. Engage in professional organization representation and benchmarking in industry networks. Provide guidance to business teams on technical regulatory requirements and lead/assist where needed. Participate in internal business and technical forums as Quality's voice for GMP material and commodity suppliers' oversight. Conduct regular review and assessment of regulatory intelligence and communicate concerns, trends, gaps, alerts to Quality management timely. Anticipate potential problems and risks related to regulatory compliance expectations globally. Approximately 20% travel is expected. Knowledge, Experience and Skills Expert in quality requirements pertaining to GMP material and commodity supplier management with strong emphasis on quality and performance management, risk identification and mitigation. In‑depth understanding and application of GMP principles, concepts, best practices and standards in the US and internationally. Demonstrated ability to develop and improve complex concepts, techniques, and standards and new applications based on quality principles and theories. In‑depth knowledge of Global requirements/standards for GMP material and commodity suppliers' life‑cycle management. Demonstrated ability to develop solutions to complex problems requiring ingenuity, creativity and innovativeness, where precedent may not exist. Excellent verbal, written, and interpersonal communication skills. Ability to interact with regulatory agencies and represent Gilead in public forums. Demonstrated experience and ability to manage a team of highly technical staff. Expert in managing resources to address competing projects and timelines. Basic Qualifications 12-15 years of relevant experience and a bachelor's degree in science or related fields; or 8+ years of relevant experience and an advanced science degree such as MS, MD, PharmD, PhD or an advanced business degree such as an MBA. Prior leadership experience in a complex organization - a must. Expert knowledge in technical and regulatory requirements pertaining to GMP material and commodity supplier management - a must. Biopharmaceutical or Pharmaceutical experience - a must. Prior experience leading Global or Local Supplier Quality organization in a global biotech or pharmaceutical company - a must. Experience with GMP material and commodity category management covering the different Gilead product modalities - preferred. 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*. * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Equal Employment Opportunity 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. Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnishing information; or (d) otherwise protected by law. 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. #J-18808-Ljbffr
    $243.1k-314.6k yearly 2d ago
  • Director, Strategy and Insights Enablement Lead (EPL)

    Genentech 4.5company rating

    San Francisco, CA jobs

    A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. US Medical, part of Genentech, is passionate about delivering on Our Promise to improve the lives of patients. We foster a culture of inclusivity, integrity, and creativity while boldly pursuing answers to the world's most complex health challenges. To achieve this, Genentech has identified establishing world-class digital medical capabilities as a key priority. The Opportunity We're looking for a Strategy and Insights Enablement Lead to digitally transform our medical organization. This role is key to driving strategy and insights generation using digital and AI tools. You'll act as the bridge between business needs and product development, defining feature roadmaps and leading crucial change management efforts for adoption. Success requires close collaboration with USM and CMG partners to align on a shared vision, evolve our systems architecture, and integrate cutting‑edge medical analytics to inform USM strategy. Key Responsibilities Strategic Insights & Data Leadership Lead the execution of US Medical's insights strategy, generating actionable insights from diverse sources, and spearhead a transformative digital insights strategy to pinpoint and address care gaps within therapeutic areas. This includes collaborating with stakeholders, leading the productization of the Medical Care Gaps Insights tool, and championing the innovative use of enterprise‑wide data, digital tools, and AI to elevate the customer experience and inform USM strategy. Advance Field Medical Insights by implementing a Comprehensive Insights Engine, an end‑to‑end module enabling dynamic capture of field insights and facilitating efficient, near real‑time aggregation, analysis, and reporting. This system will embed AI‑generated customized Next Best Actions (NBA) to empower Field Medical in identifying untapped experts, emerging trends, and unmet needs, and inform strategic decisions. Product & Process Enablement Leadership for Strategy and Insights Define clear business needs, prioritize features, and partner with Product Owners on roadmap development and execution, while also conducting thorough reviews and validations of products pre‑launch to ensure operational readiness and strategic alignment. Collaborate with stakeholders to design and seamlessly integrate tools into end‑to‑end medical workflows, lead essential process changes to foster adoption, and inform the overall medical data strategy and governance, ensuring compliant handling of medical data and overseeing the progressive evolution of priority USM insights systems architecture. Execution Excellence Demonstrate cross‑functional leadership by influencing and integrating diverse teams without direct authority, and create customer‑centric programs and solutions that meaningfully engage customers. Exhibit advanced proficiency in uniting, motivating, evaluating, guiding, and driving teams towards exceptional execution performance against digital insights plans, and provide exceptional leadership in planning and executing projects to address USM's data and information needs, while continuously tracking and optimizing the performance of digital insights initiatives. Who you are Qualifications & Experience Master's or advanced degree. 10+ years of experience in the healthcare industry. In-depth understanding of US clinical workflows. Expertise in managing and applying healthcare data (RWD, RWE, claims, EHR). Strong knowledge of AI/ML for insights and process automation, along with familiarity with digital health technology (CRM) and data privacy regulations (HIPAA). Preferred Qualifications & Experience A medical degree or prior experience in Medical Affairs is a strong plus. Location & Travel Requirements This position is based in South San Francisco, CA, and offers a hybrid schedule working in the office three days per week. Occasional travel may be required. The expected salary range for this position based on the primary location of South San Francisco, CA is $182,100 - 338,300. Actual pay will be determined based on experience, qualifications, geographic location, and other job‑related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Relocation benefits are not available for this job posting. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. #J-18808-Ljbffr
    $182.1k-338.3k yearly 4d ago
  • Senior Director, Market Access - Oncology

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    * Ensure all pricing, contracting, and market access activities meet legal, regulatory, and company policy requirements.* Establish governance and standardized processes to manage risk and maintain audit-ready documentation.* Entrenched expertise in oncology market access and the role of pricing/contracting amid policy change and large customer dynamics.* Exceptional executive communication-able to distill complex analytics into clear narratives and decisions.* Strong interpersonal skills to lead, influence, and drive consensus across diverse stakeholders.* In-depth knowledge of U.S. reimbursement across commercial and government channels; experience with GPO/provider ecosystems and integrated networks.* Advanced project management and disciplined execution.* Through understanding of adjacent functions (Managed Markets, Brand Marketing, Finance, Market Research, Medical, Legal, Contracting Operations, Global Value & Access).* Bachelor's degree required; advanced degree preferred (MBA, MPH, MS in Health Economics, PharmD, or related).* 12-14+ years of pharmaceutical/biotech experience, including significant oncology market access leadership.* Proven experience in data analysis, benchmarking, and primary market research among payers and KOLs.* Oncology product launch experience with demonstrated impact on pricing, access, and uptake.* Track record of leading teams and matrix organizations; success influencing senior executives and cross-functional partners. #J-18808-Ljbffr
    $197k-271k yearly est. 2d ago
  • Sr Director, Value & Access (PBC Strategy)

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    Sr Director, Global Value & Access (PBC Strategy) Sr Director, Global Value & Access (PBC Strategy) United States - California - Foster City Market Access & Health Economics Regular Gilead's mission is to discover, develop, and deliver therapies that will improve the lives of patients with life-threatening illnesses worldwide. Reporting to the Executive Director, Global Value and Access - LIVE ( Liver ● Inflammation ● Veklury ● Emerging Viruses), this role will: Key Responsibilities • Lead a high-performing matrix PBC GV&A team that develops and executes global market access strategies for Livdelzi in PBC, with a focus on pre-launch and launch planning. • Collaborate closely with country market teams to ensure successful launch and access for Livdelzi/indications. • Develop and implement comprehensive market access strategies across different health systems, considering payer, provider, patient, and policymaker stakeholders. • Partner with internal stakeholders in clinical development, commercial (global strategic marketing), medical affairs, and regulatory to ensure alignment on access strategies. • Represent GV&A in PBC teams within G.Ecosystem to inform program strategy, in alignment with GV&A strategy and requirements. • Guide the development and implementation of global value and access strategies, drawing on health economics, pricing models, payer landscapes, and global evidence requirements to maximize product value and patient access. • Develop and deliver presentations to senior management on access strategy and options to overcome barriers. • Track and analyze value and access performance metrics and identify global opportunities to establish, expand, and protect price and reimbursement, in collaboration with country market access teams. Knowledge, Skills and Experience We're seeking a strategic, influential leader with: • At least 12 years of experience in the biotech or pharmaceutical industry in market access related activities with experience in Global/regional/country market access. • Strong understanding of global payer environment, including coverage and reimbursement, pricing and contracting, formulary management, HTA and payment policy • Strong understanding of strategic pricing, contracting, negotiation and global pricing policy development • Strong understanding of the pharmaceutical product lifecycle and clinical development • Experience developing global V&A strategies, including developing global value messages, integrated evidence planning and creating tools to support implementation in key markets • Experience with market access launch planning and execution • Demonstrated ability in matrix environment that is globally-dispersed, and demonstrated experience to drive alignment within triad and cross-functionally in G.Ecosystem • Proven ability to lead and influence across functions and levels as well as lead cross-functional teams; skilled facilitator, negotiator, counselor, and advocate for country market access. • Hepatology and rare disease experience and market knowledge, is a plus Basic Qualifications • Bachelor's Degree and Fourteen Years' Experience OR Masters' Degree and Twelve Years' Experience OR PhD and Ten Years' Experience Share: Job Requisition ID R0045656 Full Time/Part Time Full-Time Job Level Director Click below to return to the Gilead Careers site Click below to see a list of upcoming events Click below to return to the Kite, a Gilead company Careers site #J-18808-Ljbffr
    $197k-271k yearly est. 3d ago
  • Senior Director, R&D Quality & Compliance Leader

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    A leading biopharmaceutical company in California is seeking a Senior Quality Assurance Manager with extensive experience in R&D compliance. The ideal candidate will have a strong background in managing compliance programs, leading process improvements, and mentoring teams. Proficiency in quality risk management principles and familiarity with regulatory requirements is essential. This role requires excellent communication skills and the ability to lead cross-functional teams with an emphasis on delivering results. #J-18808-Ljbffr
    $197k-271k yearly est. 5d ago
  • Director, Media Analytics - Hybrid/Remote Pharma Leader

    Amgen Sa 4.8company rating

    Thousand Oaks, CA jobs

    A leading biotechnology company is looking for a Director of Media Analytics to support analytics strategy and lead a team in Thousand Oaks, CA. The role requires strong analytical skills, leadership experience, and knowledge of media strategies. Candidates should have a doctorate, master's, or bachelor's degree with relevant analytics experience. This flexible position involves collaboration across teams to drive data-driven decisions and improve media initiatives. #J-18808-Ljbffr
    $165k-221k yearly est. 5d ago
  • Senior Director, Strategic Market Access Initiatives

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    United States - California - Foster City, CA - Regular‑time At Gilead, we've tackled diseases such as HIV, viral hepatitis, COVID‑19 and cancer for over 35 years by developing life‑changing therapies and ensuring global access. Our mission requires collaboration, determination, and relentless drive. We are looking for a passionate leader ready to make a direct impact within the U.S. Market Access organization. We believe every employee deserves a great leader. People leaders are the cornerstone of our culture and are responsible for creating an environment where each team feels included, empowered, and empowered to pursue their aspirations. Key Responsibilities Strategic Leadership & Execution Lead short‑term, high‑impact initiatives with urgency and precision, catalyzing strategic transformation within Market Access. Develop and execute cross‑functional strategies in response to evolving healthcare policies, payer dynamics, and corporate priorities. Drive scenario planning and risk mitigation strategies related to pricing, reimbursement, and access. Serve as a central coordination point across Market Access teams and broader corporate functions to ensure strategic alignment and timely execution. Support preparation for earnings calls and Quarterly Business Reviews, developing key U.S. Market Access messages, data synthesis, and response coordination. Cross‑Functional Liaison & Coordination Facilitate communication and alignment across Market Access teams on urgent initiatives, ensuring consistent implementation and awareness. Provide strategic guidance to cross‑functional partners to advance corporate-level strategies and achieve organizational goals. Executive Communication & Influence Represent the Vice President of Market Access in C‑level meetings and strategic planning sessions. Translate complex strategies into clear, actionable insights and executive‑level presentations. Build strong relationships with Market Access leadership and cross‑functional stakeholders, ensuring effective communication and responsiveness to urgent matters. Develop strategic recommendations and responses leveraging deep expertise in Market Access and policy landscapes. Basic Qualifications 14+ years of experience with a BS/BA (or equivalent) OR 12+ years with an MS/MA or MBA. Preferred Qualifications Bachelor's degree required; advanced degree (MBA, MPH, PharmD, or related) preferred. Minimum of 10 years of experience in pharmaceutical market access, pricing, reimbursement, or healthcare policy. Proven track record of leading complex, cross‑functional initiatives and influencing senior stakeholders. Deep understanding of U.S. healthcare policy, payer landscape, and pharmaceutical pricing mechanisms. Exceptional strategic thinking, analytical, and communication skills. Ability to thrive in a fast‑paced, dynamic environment with a high degree of autonomy. People Leader Accountabilities Create inclusion: model inclusive behavior and embed diversity value within team management. Develop talent: understand skills, aspirations, and potential of employees, providing coaching and growth opportunities. Empower teams: align team goals with organizational objectives and hold them to account while removing barriers. Salary range: $243,100.00 - $314,600.00. The position may also be eligible for discretionary annual bonus, stock‑based incentives, paid time off, and a benefits package that includes medical, dental, vision, and life insurance. Gilead Sciences Inc. is an equal employment opportunity employer. We celebrate diversity and are committed to an inclusive workplace. All employment decisions are made without regard to race, color, religion, national origin, sex, gender identity, sexual orientation, age, disability, veteran status, or any other protected characteristic. #J-18808-Ljbffr
    $243.1k-314.6k yearly 4d ago
  • Director of Computational Biology & AI/ML Strategy

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    A leading biopharmaceutical company located in Foster City, CA is seeking a scientific leader in Research Data Sciences. The ideal candidate will have extensive experience in computational biology and AI/ML, driving impactful data science initiatives in collaboration with multidisciplinary teams. This role involves statistical and bioinformatics analysis of multi-omics datasets to support target identification, with a competitive salary range of $226,185.00 to $292,710.00. #J-18808-Ljbffr
    $226.2k-292.7k yearly 4d ago
  • Director, Value Access & Strategy

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. 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 Kite and help create more tomorrows. In this position, you will be a critical GVA partner for two key launches of our potentially best in class CAR T in RR-MM: Execute the 4L+ iMMagine-1 Global Launch - develop the global market access strategy to support the ex‑US launch together with the key commercialization functions of Marketing, Medical Affairs, Technical Operations and the regional Access team. Prepare the 2L+ iMMagine-3 Global Launch - partner with regional (US, ACE, ICR) teams to optimize the access and reimbursement strategies for anito‑cel in 2L RR‑MM. Work closely with HEOR/RWE to ensure the production of compelling payer value evidence tools for rapid access. Key Responsibilities Key Market Access representative and lead in the Global Brand Team and Join‑GBT for anito‑cel. Partner with the Global and Regional functions of Value Access, HEOR/RWE and commercial to ensure seamless execution of the Access Strategy. Analyze future market access trends and competitor entry; advise the GBT/PT on access‑relevant endpoints, study designs, and magnitude of effect to achieve reimbursement, focusing on Kite's major markets of US, Australia, Canada, EU‑5 (ACE‑7) and Japan. Provide input into clinical development programs to capture value, align to what is meaningful to patients, support a differentiated target product profile (TPP) and ensure the right evidence is collected to support future reimbursement and pricing negotiations. Accountable for the market access and payer perspective to be reflected in cross‑functional strategies (product development, medical affairs, regulatory affairs, commercial). Partner with Health Economics Outcomes Research (HEOR), Real‑World Evidence (RWE) and Global Marketing to ensure meaningful target product profiles are developed and evidence plans are optimized to support reimbursement. Identify global HEOR evidence requirements and gaps; coordinate with HEOR to develop studies, models, and resources to support value demonstration and product differentiation for assigned indication(s). Basic Qualifications 12+ years' experience with a BS/BA (or equivalent). 10+ years' experience with an MS/MA or MBA (or equivalent). Preferred Experience Previous experience supporting product launches, ideally in oncology. Demonstrated experience in a healthcare environment, preferably the pharmaceutical industry or related consulting services. Extensive understanding of the global hematology/ multiple myeloma market access landscape, cell therapy business and healthcare system dynamics. Detailed knowledge of payer systems, pricing and reimbursement mechanisms, decision‑makers and payer stakeholder behavior for relevant markets (US, EU‑5, Japan). Knowledge of HTA assessments including value frameworks, methodologies, trends and drivers in relevant markets. Ability to guide the development plan and lead inputs based on payer requirements and market access trends. Excellent communication skills and experience in presenting at senior committees. Ability to collaborate successfully across multiple cultures and time‑zones. Demonstrated leadership in cross‑functional teams. People Leader Accountabilities Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way teams are managed. Develop Talent - understand the skills, experience, aspirations and potential of employees and coach them on current performance and future potential; ensure employees receive 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 accountable; provide the support needed to remove barriers and connect the team to the broader ecosystem. The salary range for this position is: $205,615.00 - $266,090.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation may vary. This position may also be eligible for a discretionary annual bonus, discretionary stock‑based long‑term incentives (eligibility may vary by role), paid time off, and a benefits package. Benefits include company‑sponsored medical, dental, vision and life insurance plans. For additional benefits information, visit ******************************************************************* For jobs in the United States Kite Pharma 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, 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. #J-18808-Ljbffr
    $205.6k-266.1k yearly 2d ago
  • Director, Grants & Social Impact Strategy

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    A leading biopharmaceutical company is seeking a Director of Corporate Responsibility in Foster City, California. This role involves leading grant initiatives and public relations strategies to enhance the company's philanthropic impact. Candidates should have a strong background in healthcare public relations with at least 10 years of relevant experience. The position requires excellent communication skills and the ability to manage diverse projects successfully. Competitive compensation and a supportive work environment are offered. #J-18808-Ljbffr
    $156k-201k yearly est. 5d ago
  • Director, Commercial Data Strategy & Governance

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    A leading biopharmaceutical company is seeking a Director of Data Strategy and Governance in Foster City, CA. This role involves leading data acquisition strategies and managing data governance for commercial operations, with a strong focus on oncology. Candidates should possess over 12 years of experience, exceptional project management skills, and a solid understanding of pharmaceutical data systems. This position can be hybrid if located in the Pacific Time Zone. #J-18808-Ljbffr
    $156k-201k yearly est. 5d ago
  • Director, Data Strategy and Governance (Commercial Therapeutic Data Strategy)

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    United States - California - Foster City Commercial/Sales Operations Regular Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. We strive to transform and simplify care for people with life-threatening illnesses around the world. Gilead's portfolio of products and pipeline of investigational drugs includes treatments for HIV/AIDS, COVID, HBV, HCV, HDV, Oncology and Cell Therapy as well as Inflammatory Diseases co. Gilead is a patient centric, science focused company. This position reports to the Head of Data Strategy & Governance. Data is the key driver of business decisions for the Commercial organization at Gilead. This position is responsible for data strategy and acquisition for all therapeutic areas. This position will drive the data strategy for both internally available data as well as leveraging external partnerships. This position is responsible for leading commercial operations to the next level from a data strategy perspective. With significant budget responsibilities, this role will be the point of contact for all of commercial for data acquisition across all third-party data suppliers. This position is site based at our Global Headquarters in Foster City, CA (We will consider remote if you are in the Pacific Time Zone and can travel to Foster City as needed). Core job responsibilities include: Lead Data acquisition for US working closely with US analytics, GDSI analytics, Data Science, and US marketing teams. Run the US data governance for new purchases, deleting purchases. Own data strategy & acquisition workstreams from end to end which includes but not limited to developing data strategy, acquiring budgets / approvals, working with vendor partners for creating long term partnerships as well as running proof of concept analytical projects. Drive quarterly / yearly data strategy sessions with the brand marketing and sales partners Work with vendors to evaluate data options for the Commercial Team Lead Specialty pharmacy data strategy along with patient data strategy for all therapeutic areas Develop best-in‑class data strategy model for product launches [pipeline to commercial] Responsible for all budget management [accruals, forecast, cross charges etc] for a significant dollar amount Build business cases for new and exploratory data assets Drive analytical proof of concepts for new data assets and establish long term partnerships for successful POCs. Partners with IT, Analytics and other Commercial Operations stakeholders on building key Commercial systems and processes such as Commercial Data Warehouse (Lake) Explore new technologies to innovate and help other team members in areas of data investigations, data conflicts, manual data steward queue etc. Work closely with legal to establish DLAs with advertising partners Support advanced analytical capabilities from a data perspective. Knowledge & Skills Strong project management skills and demonstrated ability to drive large and complex cross‑functional projects and sustain them long term. Strong working knowledge of relevant software systems (e.g. MS Excel, Access, MS Word & PowerPoint, etc.) is required Knowledge of SQL, and/or other BI tools (MicroStrategy, Tableau, etc.) is required Ability to work with and coordinate demands from multiple internal customers; highly collaborative Demonstrated excellence in strategic and tactical analysis and proactive planning. Ability to recognize and interpret business issues/opportunities and recommend solutions through analysis / proof of concepts. Ability to present complex information in an accurate and persuasive manner to all levels of management. Ability to effectively communicate technical and qualitative information to non‑technical executives through interpersonal, verbal, and written channels. Deep knowledge of pharmaceutical data (specialty pharmacy, wholesaler data, Symphony and IQVIA offerings, etc) and systems (CRM, Customer Master, Data Warehouse, Sample systems, etc.) Understanding/awareness of the Pharmaceutical business model (Product Development, Marketing, Sales, Sales Operations, Marketing Analytics, Medical Affairs, Contracting etc) Run monthly communications for new data purchases and upcoming data needs for US Highly visible position accountable for all data that supports across Commercial 12+ years of relevant experience with Bachelor's Degree. MBA or other related graduate‑level degree is a plus 6 or more years of work experience in data strategy and commercial acquisition Previous experience in oncology/hematology is required Exceptional ability to manage multiple projects in a fast‑moving entrepreneurial environment, with changing priorities and significant time pressures Strong communication skills (both verbal and written) required. Demonstrated ability to collaborate and work cross‑functionally Ability to develop and maintain strong team, including external partners, relationships while driving for positive results. Possess a willingness and ability to work hands‑on and with a sense of urgency Extensive proficiency with Microsoft Office (Word, Excel, PowerPoint and Outlook) and forecasting software (e.g., Crystal ball, Forecast Pro, customized platforms) #J-18808-Ljbffr
    $156k-201k yearly est. 5d ago
  • Director, US Medical Affairs Strategy & Execution

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    A leading biopharmaceutical company is seeking a Director for USMA Strategic Execution. This role focuses on operationalizing medical strategy across therapeutic areas, requiring proven experience in the pharmaceutical industry, strategic execution, and leadership. Candidates should hold a relevant degree and possess strong skills in project management, influence, and communication. The position is based in either Foster City, CA, or Parsippany, NJ, and offers a competitive salary. #J-18808-Ljbffr
    $156k-201k yearly est. 2d ago
  • Director, End-to-End Product Supply Chain & Strategy

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    A leading biotechnology company is seeking a Director - E2E Product Supply Chain to lead and optimize their supply chain operations. The candidate should have at least 10 years of experience in Supply Chain, with a strong focus on compliance and operational excellence. This role involves developing supply chain strategies, overseeing demand planning, and ensuring high standards of quality and efficiency. The ideal candidate excels in analytical skills and has proven leadership experience within the industry. #J-18808-Ljbffr
    $156k-201k yearly est. 2d ago
  • Director, Global Commercial Product Strategy, Hepatitis C

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    Reporting to the Executive Director, Established Products, this role is responsible for leading the global commercial strategy, positioning, and execution for Hepatitis brands. The successful candidate will be responsible for close collaboration with cross-functional teams and markets to ensure impactful and innovative strategies that address unmet needs, drive product differentiation, and deliver on global brand objectives. Key Responsibilities Develop and implement annual commercial plans that inform and guide country-specific brand plans. Identify actionable insights through market research to address unmet needs and enhance product differentiation. Collaborate with clinical and medical affairs teams to develop and execute data generation strategies that support brand objectives. Oversee the development and approval of promotional materials, including message development when new data, such as real-world evidence (RWE), becomes available. Design and implement innovative non-personal promotion (NPP) strategies in partnership with digital and innovation. Support the creation of materials for forecasting, long-range planning (LRP), global LE, and budget guidance. Lead and execute commercial projects and congress participation, ensuring alignment with the plan of action (POA). Cross-Functional Collaboration Engage and collaborate with local markets, Medical Affairs, Value and Access, Analytics and Insights, Competitive Intelligence, Commercial Operations, Clinical Development, Governmental Affairs, and Public Affairs to align on and implement global marketing strategies. Lead the Epclusa Established Products Team (EPT) Partner with PDM, Trade Operations, Regulatory Affairs, and Medical Affairs to drive key initiatives, including competitive updates and formulation development. Business Optimization & Market Support Support developing business cases for new and identified opportunities. Facilitate monthly forums to align affiliates on global strategies, share best practices, and provide guidance. Provide proactive guidance on regional business decision-making, including ATU analysis and in-market POA development. Support strategic initiatives such as maximizing product differentiation and penetration in key markets. Drive impactful commercial initiatives aligned with global strategic imperatives. Support ongoing projects and ensure seamless implementation of innovations. Basic Qualifications Bachelor's Degree and Twelve Years' Experience OR Masters' Degree and Ten Years' Experience OR PhD and Eight Years' Experience Preferred Qualifications At least 12 years of relevant commercial experience in the biotech or pharmaceutical industry, including global product strategic planning, portfolio and lifecycle brand management, tactical marketing, and product planning and launches Liver/Rare Disease-specific experience and market knowledge (preferred) Prior regional or global experience (preferred) Strong ability to influence and lead cross-functionally to drive the business. Competitive mindset and ability to focus and prioritize. Strong analytical skills with the ability to derive actionable insights from market research and data. Excellent project management skills and experience managing multiple stakeholders across diverse geographies. Strategic mindset with a focus on innovation and delivering measurable outcomes. Proven ability to effectively operate in a fast-paced environment with high expectations and a customer focus which drives the need for quality deliverables and performance. Demonstrated teamwork and excellence in project management working collaboratively with key stakeholders while effectively managing multiple priorities and projects Outstanding ability to influence and lead cross-functionally to drive the business Strong analytical skills, demonstrated by the ability to identify trends and provide appropriate recommendations Proven ability to effectively operate in a fast-paced environment with high expectations and a customer focus which drives the need for quality deliverables and performance Competitive mindset, and demonstrated ability to prioritize, focus and create an impact in market and for patients Gilead Core Values Integrity (Doing What's Right) Inclusion (Encouraging Diversity) Teamwork (Working Together) Excellence (Being Your Best) Accountability (Taking Personal Responsibility) Share: Job Requisition ID R0044882 Full Time/Part Time Full-Time Job Level Director Click below to return to the Gilead Careers site Click below to see a list of upcoming events Click below to return to the Kite, a Gilead company Careers site #J-18808-Ljbffr
    $156k-201k yearly est. 1d ago
  • Senior/Principal Business Manager- Translational Medicine

    Genentech 4.5company rating

    San Francisco, CA jobs

    We advance science so that we all have more time with the people we love. The Senior/ Principal Business Manager will serve as a strategic advisor and thought partner to senior leadership within the gRED Translational Medicine organization. This individual will play a critical role in driving cross-functional alignment, enabling business planning and operational excellence, and ensuring the successful execution of strategic priorities. The role requires strong business acumen, systems thinking, and the ability to influence and partner across multiple levels and functions. The Business Manager also enables leadership team effectiveness by shaping agendas, connecting strategic dots, and anticipating organizational needs. With a strong grasp of the enterprise landscape, the Senior Business Manager proactively connects strategic priorities to execution, facilitates sound decision-making, and identifies opportunities to strengthen how the organization operates, collaborates, and delivers impact. The Opportunity: As a valuable member on the Translational Medicine team you will be: Serving as a strategic thought partner to senior functional leaders (Director and Vice President level), providing insights and driving aligned decision-making in support of organizational goals. Leading short- and long-term business planning efforts, including annual planning cycles, resource allocation, budget forecasting, and functional goal setting. Driving leadership team operating rhythm, ensuring effective prioritization, focus, and delivery on strategic objectives. Anticipating emerging needs, risks, and opportunities across the organization and proactively frames options for leadership consideration. Facilitating effective leadership and project team operations-designing and executing agendas, preparing briefing materials, and ensuring clarity of decisions, follow-ups, and outcomes. Connecting the dots across initiatives and stakeholders, identifying interdependencies and proactively addressing risks and opportunities. Synthesizing data and perspectives to support informed decision-making, including preparing pre-reads, strategic recommendations, and decision frameworks for leadership discussions. Driving planning and execution of strategic initiatives and change efforts that support the function's success and alignment with gRED and enterprise priorities. Advising on and contributing to solutions for complex challenges, offering structure, process, and creative thinking to move initiatives forward. Supporting key people and culture activities-such as functional offsites, recognition programs, and engagement initiatives-helping to foster a high-performance, inclusive, and purpose-driven environment. Acting as a connector across teams, promoting collaboration, shared accountability, and alignment toward common goals. Supporting communication strategies to ensure transparency, clarity, and engagement across stakeholders and organizational levels. Bringing a strong enterprise mindset, continuously linking functional goals to broader strategic context and organizational objectives. Who You Are A skilled communicator with strong written, verbal, and presentation abilities-able to synthesize and convey complex information clearly and effectively to diverse audiences. Highly organized, with exceptional program and project management capabilities. Trusted relationship builder who fosters collaboration, psychological safety, and transparency across teams and leadership levels. Agile and resourceful in navigating ambiguity and shifting priorities, with a proactive and solutions-oriented mindset. Adept at identifying process improvements and delivering business impact through operational excellence. Demonstrated experience in business management disciplines such as: Strategic planning Organizational development Project and portfolio management Business process improvement Change management Internal communications and engagement Proven success leading cross-functional initiatives in complex matrixed environments. Background in clinical development, drug development, or translational research is preferred. Strong understanding of enterprise functions, organizational dynamics, and business operations. Formal degree preferred; equivalent training and experience will be considered. Additional training or certification (e.g., PMP, Six Sigma, Design Thinking, Agile) is a plus. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of California for Senior Business Manager is $144,000- $267,400 and Principal Business Manager is $156,500-$290,700. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company\'s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. #J-18808-Ljbffr
    $156.5k-290.7k yearly 4d ago
  • Director, Corporate Responsibility

    Gilead Sciences, Inc. 4.5company rating

    Senior director job at Gilead Sciences

    United States - California - Foster City Public Affairs/Communications Regular Gilead's mission is to discover, develop, and deliver therapies that will improve the lives of patients with life‑threatening illnesses worldwide. As the Director, Gilead Sciences, Corporate Responsibility, you will report to the Executive Director and will primarily lead the grants portfolio across the Gilead Foundation's strategic initiatives, including the Healthcare Education Access and Leadership (HEAL) initiative, the Creating Possible Fund, and other programs and projects. Essential Duties and Job Functions: Grantmaking Foster and maintain effective relationships with grantees, non‑profit leaders, and the philanthropic community. Identify additional collaborative opportunities among grantees and other local organizations. Support overall grantee development; create and implement capacity‑building opportunities for grantees through webinars, workshops, and cohort meetings; act as a strategic thought partner to grantees. Work with the executive director and grantmaking team to assess and determine best ways to respond to emerging opportunities and challenges through grantmaking activities and the design and implementation of programs that support the Gilead Foundation's mission. Develop and manage grantmaking processes, including developing grantmaking guidelines and Funding Opportunity Announcements, staff review of proposals, and preparation of dockets for board review. Evaluation Lead effective evaluation and impact reporting plans, working collaboratively with grantees. Oversee grant agreements, reporting requirements, and financial stewardship of grantees. Support the development and implementation of a system to track progress and impact of all strategic initiatives and grants. Collaborate with Gilead Foundation and Gilead Sciences learning and evaluation staff and vendors to refine knowledge management and grant evaluation systems. Work effectively with Gilead Foundation vendors and consultants, including overseeing contracts, invoices, scope of work, and ensuring on‑time completion of deliverables. Communications Develop strategic and tactical plans to bring strategic initiatives to life, with goals aligned with mission and priorities, working in close collaboration with Gilead Sciences communications and public relations colleagues. Communicate the Foundation's philanthropic strategy and impact to multiple internal and external constituencies; draft grant write‑ups, periodic program reports, and briefing papers; work collaboratively with Corporate Communications to share impact. Ensure the driving of integrated storytelling and editorial themes across social impact and philanthropic communications outlets, in close collaboration with Corporate Communications. Other Manage partnerships with select stakeholders to position Gilead Foundation as a thought leader and enable connections and partnership opportunities across the ecosystem. Provide general support to Gilead Foundation Executive Director and colleagues to execute overall priorities, program agenda and activities. Remain informed on current trends in philanthropy, nonprofits and issue‑specific fields, health and healthcare workforce development. Attend and participate in appropriate joint efforts and affinity group meetings, conferences, events, and networks of foundations and community partners to establish positioning in the philanthropic and issue‑specific fields. Additional Job Responsibilities Responsible for public relations programming within the Public Affairs group, supporting the company's growing portfolio of products and pipeline programs. Effectively manage all aspects of public relations agency relationships, such as providing direction and project management. May manage department staff, as appropriate. Manage budgets to target. Collaborate and regularly participate as a member of cross‑functional teams, representing external communications function; provide public relations recommendations to help achieve company goals. Develop and implement media relations strategies for specific areas of responsibility, such as product and/or corporate‑related initiatives. Serve as media spokesperson for product and/or corporate news; respond to media requests and arrange interviews with management and opinion‑leader spokespeople as appropriate. Examine complex issues from a broader organization perspective, determine communications opportunities and help determine priorities within the Public Affairs group. Prepare press releases, presentations, and other communications materials with minimal oversight. Knowledge Demonstrated experience in media relations; knowledge of industry media and reporting trends. Demonstrated knowledge of regulations and principles specific to communications for a publicly‑traded biopharmaceutical company. Must have experience with public relations tactics and resources and the relationship of those tactics to other department roles and functions, including marketing, medical affairs, government affairs and investor relations. Experience managing multiple projects (timelines, budgets, priorities) simultaneously. Excellent verbal, written, and interpersonal communication skills. Specific Education & Experience Requirements BA degree in communications, liberal arts, business or science‑oriented field and minimum 10 years of relevant experience, which includes 8‑10 years of healthcare public relations experience. Extensive knowledge of Gilead's areas of therapeutic focus is preferred. 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 R0047236 Full Time Job Level: Director #J-18808-Ljbffr
    $163k-226k yearly est. 5d ago

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