Jobs / United States / Gilead Sciences INC

Gilead Sciences INC

Manager, U.S. Medical Affairs Liver Strategy

United States - California - Foster City Posted yesterday

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Skills this job asks for

TranslationCommunicationCompliance

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Sponsorship verdict

Sponsorship possible

One solid signal, not two. Worth applying, and worth asking about sponsorship early.

  • Employer is on a government sponsor recordThe US Department of Labor certified 159 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
  • What Gilead Sciences INC paid sponsored hires in similar roles10 certified filings for “Senior Clinical Pharmacology Manager” (Medical Scientists, Except Epidemiologists) in CA: $127k–$184k, median $159k.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Employer is on a government sponsor record
The US Department of Labor certified 159 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. Source: LCA disclosure data (US Department of Labor (OFLC)).
No salary bar for this route
H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
What Gilead Sciences INC paid sponsored hires in similar roles
10 certified filings for “Senior Clinical Pharmacology Manager” (Medical Scientists, Except Epidemiologists) in CA: $127k–$184k, median $159k. Most were filed at wage level II (40%) — 2 lottery entries, ≈31% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).

US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

About the role

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   At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.  We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come.  As a Manager, U.S. Medical Affairs, Liver Strategy at Gilead you will report to the Executive Director, Head USMA Liver Group and will support the development, management, and execution of U.S. Medical Affairs liver strategy in PBC, HDV, and across the portfolio. The Manager will play a critical role in translating USMA Liver strategy into high-quality, scientifically rigorous, compliant, and field-ready medical materials, digital resources, conference/symposium deliverables, and cross-functional planning initiatives. This individual will support across-portfolio content creation and lifecycle management through Medical Review Committee (MRC), help manage digital and AI-enabled medical platforms, and contribute to congress, conference, and symposium strategy and execution. The ideal candidate is scientifically minded, creative, highly organized, and able to manage multiple priorities in a fast-paced, matrixed environment. This person should have strong Medical Affairs content experience, outstanding written and verbal communication skills, and the ability to work collaboratively across USMA Liver, Field Medical, Global Medical Affairs (GMA), Medical Information, Legal, Compliance, Commercial, Training, Operations, and external agency partners. This role is based in Foster City, California. Essential Duties and Responsibilities: • Support the development and execution of USMA Liver strategy across key liver disease priorities, including PBC, HDV, other viral hepatitis, and emerging portfolio needs. • Work in close partnership with more senior team members on USMA Liver strategy and translation of strategy to content • Serve as a key content and scientific contributor for USMA Liver, helping translate complex clinical, real-world, guideline, and congress data into clear, balanced, compliant medical communications. • Lead or support creation, revision, review, approval, deployment, and lifecycle management of USMA Liver medical materials, including scientific slide decks, field-facing resources, FAQs, training materials, advisory board content, congress summaries, symposia materials, and digital me

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