Exec Director, Global Regulatory Strategy Head of Inflammation
$302.01k - $390.83kGilead 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.
Job Description
Key Responsibilities
Provide leadership to the global inflammation regulatory organization to advance Gilead's portfolio across the full product lifecycle, from Phase I through Phase IV, in alignment with corporate objectives.
Leverage in-depth regulatory knowledge and inflammation expertise to deliver strategic and technical guidance, including innovative and precedent-informed regulatory approaches to global registration.
Dissect and distill complex regulatory issues to provide clear strategic direction and support interactions with health authorities, including preparation of high-quality regulatory content.
Hire, develop, and retain diverse top talent; set clear and aspirational goals; and coach direct reports on performance, development, and career progression.
Foster a culture of excellence and innovation, empowering teams to perform at their highest potential.
Own and manage departmental budget and resource planning.
Build, maintain, and strengthen partnerships across Development, PDM, and Commercial functions to support near-term regulatory execution and long-term strategic vision.
Represent GRA at Development Review Committees (DRCs) and provide impactful regulatory leadership to support robust development plans.
Provide regulatory oversight and guidance for due diligences related to in-licensing, external collaborations, and acquisitions.
Contribute as a member of the Global Regulatory Affairs Leadership Team to regulatory vision, roadmaps, initiatives, and outcomes.
Ensure all activities are conducted in full compliance with applicable laws, regulations, ICH guidelines, regional requirements, and internal policies and SOPs.
Maintain strong awareness of the external regulatory landscape and evolving requirements impacting Gilead's portfolio.
Develop and champion high-impact initiatives that advance the regulatory function and enterprise goals.
Qualifications
Advanced science degree (PhD, PharmD, MD, or MSc) with 14+ years, or Science Degree (BSc) with 16+ years of experience and regulatory leadership experience, including leadership of global teams.
Deep expertise in the inflammation therapeutic area, ideally gained through regulatory leadership of multiple global development programs and lifecycle management activities, including NDA/MAA submissions.
Proven ability to represent the company in complex negotiations with regulatory authorities in the US, EU, Japan, China, and other regions.
Strong influence, interpersonal and communication skills, with the ability to collaborate effectively across functions.
Extensive knowledge of global regulatory requirements, including ICH and regional frameworks, and the ability to assess their impact on business strategy.
Demonstrated capability to lead transformational initiatives in response to evolving legislation and regulatory expectations.
Ability to critically review complex scientific and technical documents and influence decision-making across matrixed organizations.
Strong executive presence with the ability to navigate senior-level stakeholder environments effectively.
Recognized internally and externally as an expert regulatory resource.
The salary range for this position is: $302,005.00 - $390,830.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
- Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
For jobs in the United States:
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact View email address on click.appcast.io for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' ( poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT (
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
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 a 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 furnish 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.
For Current Gilead Employees and Contractors:
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.
$349.01k
...limited to): Provide global Medical Affairs... ...GMA and Development TA Heads, and other members of... ...appropriate lifecycle research strategy (eg market archetype... ...Clinical Development, Regulatory Affairs, Patient... ...: virology, oncology, inflammation and/or hepatology....SuggestedFor contractorsLocal areaWorldwide$349.01k
...Responsibilities Provide global Medical Affairs... ...GMA and Development TA Heads, and other members of... ...appropriate lifecycle research strategy (eg market archetype... ...Clinical Development, Regulatory Affairs, Patient... ...: virology, oncology, inflammation and/or hepatology....Suggested$281.01k - $363.66k
...Government Affairs, and engages colleagues across Public Affairs' global centers of excellence to help inform cross-functional... ...Affairs and Government Affairs to help drive cross-functional strategy and tactical plans that assert Gilead's longstanding leadership...SuggestedFor contractorsLocal area$174k - $203k
...Summary: The Associate Director for Drug Substance (DS) Commercialization... ...cross-functional efforts for regulatory filings, and commercial... ...into the Senior Director for Global DS Commercialization, Protein... ...on overall program strategy, with primary responsibility...SuggestedRemote work- ...position holder will be Director, Human Resource Business... ...to support the assigned Global R&D functions, i.e. Global Regulatory Affairs organization as well... ...mid/long-term HR/talent strategy and implementation plan according... ..., guide departmental heads, management, and...Suggested
$186k - $233k
...framework that supports international growth and regulatory compliance. Lead oversight and expansion of core quality systems across global sites, including document control, GxP... ...and executive leadership on quality strategy and risk-based decision making. Deep knowledge...Full timeLocal areaFlexible hours$243.1k - $314.6k
...Director, Global Medical Affairs, Hepatitis B and C At Gilead, we're... ...position within the Global Liver Inflammation, Respiratory Virology and... ...the Medical Affairs strategy for the HBV and HCV therapeutic... ...with Market Access, Regulatory Affairs, Country Medical Director...Local area$211k - $264k
...signaling pathway. The Opportunity: The Director, Global Medical Affairs will report to the GI Tumors Medical Affairs Strategy Lead and will be responsible for supporting... ...Program Management, Business Development, Regulatory, Safety, and Compliance teams. The ideal...Full timeLocal area$244k - $305k
...Opportunity: Reporting to the GI Tumors Medical Affairs Strategy Lead, the Senior Director, Global Medical Affairs, will be responsible for developing... ...Operations, Program Management, Business Development, Regulatory, Safety, and Compliance teams. Required Skills,...Full timeLocal area$243.1k - $314.6k
...Reporting to the Sr. Director of Hepatitis B and C, Global Medical Affairs, this role... ...within the Global Liver Inflammation, respiratory Virology and... ...driving the Medical Affairs strategy for the HBV and HCV... ...coordination with Market Access, Regulatory Affairs, Country Medical...For contractorsLocal area$340k - $370k
...VP Of Regulatory And Head Of Regulatory Affairs The VP of Regulatory and Head of Regulatory... ...Affairs will shape and execute regulatory strategies and lead and manage submissions to... ...will serve as the primary liaison with global regulatory authorities and involve close...$210.38k - $272.25k
...Director, Global Trade Compliance At Gilead, we're creating a healthier world for all people... ...Legal, Tax, and Finance, ensuring regulatory compliance, financial integrity, and optimized... ...execute the global trade compliance strategy aligned to corporate, supply chain,...Contract work$134.5k - $215.4k
...Description Interchange is central to Visa's business, and the Global Interchange Compliance team collaborates with the broader... ...Analyst, Global Interchange Compliance role will support interchange strategy by ensuring proper levels of interchange are paid and received...Work experience placementWork at officeLocal areaRemote workWork visa3 days per week- ...BeOne is a global biopharmaceutical company dedicated to the discovery and development of innovative drug therapies for the treatment... ...BeOne global team. General Description: The Executive Director, Strategy & Business Operations, Global R&D Technology Solutions is...Shift work
- ...The Position Head of Digital Strategy, Excellence & Standards, Global Digital & Data Analytics Why Roche At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine...Local area
$180k - $220k
...Director, Strategic Insights At Franklin Templeton, we're advancing our industry forward... ...inclusive, and flexible culture to our global and diverse business, we provide... ...candidate with a management consulting or strategy background who excels at navigating ambiguity...Work at officeRemote workFlexible hoursShift work- ...Executive Director or Vice President, Global Privacy About the Company Esteemed life science company developing innovative medical products... ...development and implementation of a comprehensive global privacy strategy. The successful candidate will be a senior leader with a...Worldwide
- ...General Description: The Director, Global Regulatory Lead, will be responsible for developing, implementing, and advising on global regulatory strategies for development programs to secure and maintain market access for product(s) in line with business objectives,...Temporary workWork experience placementShift work
$163.4k - $223.4k
...position holder will be Director, Human Resource Business... ...to support the assigned Global R&D functions, i.e. Global Regulatory Affairs organization as well... ...mid/long-term HR/talent strategy and implementation plan according... ..., guide departmental heads, management, and...Hourly payFull timeLocal areaWorldwide$180k - $210.5k
...activities. This role develops and executes multi-product global regulatory CMC strategies for investigational products and leads the preparation... ...Canada and ICH) guidelines Reports to: Executive Director, CMC Regulatory Location: San Carlos, CA / US Remote...Remote work$93 per hour
...currently looking for: a Senior Director, Oracle Alliance to own the... ...business development, offer strategy, co-sell execution, partner enablement... ...engagement cadence — QBRs, exec sponsor meetings, steering... ...Message Video Phone™ (MVP™) global platform. More flexible and...Full timeWork experience placementFlexible hours$93 per hour
...currently looking for: a Senior Director, AI & SI Alliances to own and... ...business development, offer strategy, go-to-market execution,... ...hyperscalers, AI platform vendors) and Global/Regional SIs; serve as... ...structured engagement cadence — QBRs, exec sponsor meetings, steering...Full timeWork experience placementFlexible hours- ...Associate Director, Cmc Regulatory Affairs For Biologics At Gilead, we're creating... ...for defining regulatory strategy for one or more molecules... ...ensure "right first time" global approvals of Cmc regulatory... ...meetings support regional heads, as necessary. Provide input...Local area
$205k - $225k
...Associate Director, Regulatory Affairs Advertising and Promotion Foster City Mission... ...role is accountable for helping develop strategies and timelines, and managing internal team... ...This role will report to the Director, Global Regulatory Affairs Advertising and Promotion...Work at officeLocal area- ...We are recruiting on behalf of a global clinical stage biotech who are looking to hire an Associate Director Regulatory Affairs to join their team on a permanent basis. Working... ...the effective implementation of regulatory strategies. Key Responsibilities Serve as...Permanent employment3 days per week
$182.07k - $235.62k
...help create possible, together. Job Description Associate Director, Ethics & Compliance Advisor, HIV Treatment Ethics and... ...compliance and integrity into Gilead’s culture. Help drive global consistency in our compliance program, and ensure best practices...For contractorsLocal areaWorldwide$186k - $233k
...RAS signaling pathway. The Opportunity: The Associate Director, Global Regulatory Affairs Project Management is an integral part of the... ...organization and is responsible for translating global regulatory strategies into actionable execution plans. This role applies...Full timeWork at officeLocal area- ...manage, evaluate, and complete regulatory projects consistent with... ..., and advising on regulatory strategies for development programs to secure... ...are met. The Associate Director will also manage regulatory aspects... ...IND/CTA, NDA/MAA, and other global submission documents in...
- ...Position Summary: The AD, Regulatory Affairs CMC, is responsible for developing and implementing global regulatory CMC strategies to secure and maintain market access for assigned product(s) in line with business objectives, and in coordination with key internal stakeholders...Contract workLocal area
$188.4k - $301.5k
...transformational leader to join our team as the Director of Onsite Technology Support. The ideal... ...goals and align with technology strategy. Be an exemplary leader, embodying the... ...~6+ years Previous experience managing globally diverse support teams. ~ Previous executive...Work experience placementWork at officeLocal areaShift work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Exec Director, Global Regulatory Strategy Head of Inflammation. Be the first to apply!
- director global regulatory affairs San Mateo, CA
- regulatory & compliance manager San Mateo, CA
- compliance manager San Mateo, CA
- head compliance San Mateo, CA
- compliance director San Mateo, CA
- regulatory affairs director San Mateo, CA
- regulatory manager San Mateo, CA
- manager regulatory affairs San Mateo, CA
- director strategy and innovation San Mateo, CA
- planning supervisor San Mateo, CA

