Gilead Sciences · 14 hours ago
Senior Director, Product Management Team Lead (Late Phase & Commercialization) – Foster City
San Francisco Bay Area
Full-time
Onsite
Director/Executive
$243K/yr - $315K/yr
10+ years expGilead Sciences is a biopharmaceutical company dedicated to creating a healthier world by developing therapies for life-threatening diseases. The Senior Director, Product Management Team Lead will lead a team of product and project management professionals, focusing on late-phase biopharma programs and contributing to broader organizational priorities.
BiopharmaBiotechnologyHealth CareManufacturingPharmaceutical
Responsibilities
Lead team of PMs to support our PDM Product Strategy Leads and Product Teams. This includes identifying and sharing best practices across the Product Strategy Teams
Serve as SME on late phase PM, drawing upon deep knowledge of late phase, including launch planning and early commercialization product milestones
Use and provide feedback on a set of templated tools and processes for the PDM Team System, e.g. tools for capturing a product’s strategy on a single page
Work in partnership with the PDM Product Strategy Leads to develop, gain approval for, and execute on the product strategy for our products, including key milestones, budgeting and resource allocation
Support PDM Operations Management’s implementation and iteration of G.Plan (Planisware) and G. Plan product templates. Support the flow of accurate data into PDM milestone planning and resource-allocation tools (G.Plan)
Support PDM Operations Management’s and PDM Finance’s collection of product budget information by implementing processes for PMs to collect budget info on a per product basis
Support PDM Operations Management’s product portfolio reporting & analytics
Support and manage Director-level PM’s work on non-product projects
Lead, coach and develop PMs at various career levels
Qualification
Required
A degree in life sciences or a relevant business area with 14+ years of varied post-graduation experience in Pharmaceuticals, Biosciences or a related industry. Or MS with 12+ years of relevant experience. Or PhD with 10+ years of relevant experience
Proven track record of successfully PM'ing late phase and commercialization-stage biopharma programs, working with Clinical Development and Commercial teams
Demonstrated experience coordinating and leading cross-functional activities in support of BLA filings. This includes developing and managing integrated project plans, aligning regulatory and technical workstreams, and ensuring timely delivery of high-quality submission components
Possess strong business acumen to align drug development and launch strategies with commercial goals, assess financial implications, and support data-driven decision-making across the portfolio
Proven experience leading E2E TT activities across all stages of the biopharma lifecycle—from early development through commercial manufacturing. Demonstrated ability to manage complex tech transfers to and between CDMOs, including oversight of timelines, risk mitigation, documentation, and cross-functional coordination
Skilled in navigating global regulatory expectations, ensuring knowledge continuity, and driving operational readiness to enable successful manufacturing execution
Possess basic understanding of clinical trial design and its ramifications for IMP demand planning
Demonstrated ability to partner with product / project leaders to set vision and strategy for cross-functional teams
Demonstrated capability to navigate and lead in a highly networked environment and experienced with the required elevated level of influencing skills
Expertise in developing and managing project scope, deliverables, risks and resource requirements
Excellent analytical skills with an ability to summarize and present complex information in a clear and concise manner
Outstanding verbal and written communication skills with the ability to effectively interact with all levels within the organization
Must be able to understand and communicate scientific and business elements associated with pharmaceutical / biotech products
Experience leading and supervising PM teams
Leadership qualities of the successful candidate include the following: Business acumen, collaboration, building and developing high performing teams, accountability, cross-functional engagement and influence, program management, strategic vision, executive presence, coaching, goal setting and performance management. Demonstrated ability to lead without authority, influence and motivate teams
Benefits
Discretionary annual bonus
Discretionary stock-based long-term incentives (eligibility may vary based on role)
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans
Company
Gilead Sciences
Gilead Sciences is a biopharmaceutical company that discovers, develops, manufactures and commercializes therapies for critical diseases.
10001+ employees
H1B Sponsorship
Gilead Sciences has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (269)
2024 (241)
2023 (222)
2022 (208)
2021 (235)
2020 (187)
Funding
Current Stage
Public CompanyTotal Funding
$4.41BKey Investors
Abingworth
2024-11-13Post Ipo Debt· $3.5M
2024-02-29Post Ipo Equity· $210M
2023-09-07Post Ipo Debt· $2B
Leadership Team
Keeley Wettan
Senior Vice President, Legal
Patrick Loerch
Senior Vice President, Clinical Data Science
Recent News
2026-01-09
2026-01-08
2026-01-07
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