Jobs / United States / Gilead Sciences INC

Associate Director, Multiple Myeloma, U.S. Medical Affairs

Gilead Sciences INC · 🇺🇸 4 Locations

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. USCIS also records 75 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
  • 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. 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 roles2 certified filings for “Associate Director, Patient Safety” (Medical and Health Services Managers) in CA: $209k–$226k, median $217k. Most were filed at wage level IV (100%) — 4 lottery entries, ≈61% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
  • Confirmed live todayWhen a source last listed this job as open.

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.

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Sponsor Radar — Gilead Sciences INC

159 H-1B filings certified since Oct 2025

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. USCIS also records 75 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).

Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Gilead Sciences INC →

About the role

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. Job Description An exciting opportunity has arisen to join the U.S. Medical Affairs Team with a focus on Multiple Myeloma. In this role, you will contribute to advancing innovative therapies in one of the most rapidly evolving areas of oncology and help improve outcomes for patients living with multiple myeloma.   We are seeking a highly motivated individual to join our U.S. Medical Affairs team as an Associate Director, Multiple Myeloma. This role will support the execution of the U.S. Medical Affairs strategy within the myeloma portfolio, including emerging cellular therapy programs. The successful candidate will work cross-functionally with stakeholders across Field Medical, Commercial, Market Access, HEOR/RWE, Clinical Development, and Global Medical Affairs to deliver impactful medical initiatives that support scientific exchange, evidence generation, and launch readiness.   This position will report to the U.S. Multiple Myeloma Medical Lead. Position will be filled and report into Foster City, CA, El Segundo, CA, Thousand Oaks, CA, or Parsippany, NJ.   Job Responsibilities • Independently lead priority workstreams while contributing to the development and execution of the U.S. Multiple Myeloma Medical Affairs strategy. • Serve as a strategic medical partner to Field Medical, Commercial, Market Access, HEOR/RWE, Clinical Development, Regulatory, Safety, and Global Medical Affairs teams. • Translate clinical data, treatment landscape insights, competitive intelligence, and stakeholder feedback into actionable medical strategies and evidence-generation opportunities. • Support the development and refinement of scientific communication platforms, core medical content, FAQs, presentations, and field-facing resources that enable compliant scientific exchange. • Lead or support advisory boards, expert engagement activities, congress initiatives, symposia, medical education programs, and stakeholder events aligned with medical objectives. • Partner closely with Field Medical to drive scientific engagement, insight generation, launch readiness activities, and execution of medical priorities. • Represent U.S. Medical Affairs in cross-functional forums, disease-area teams, governance discussions, and launch planning activities. • Provide medical review and approval of promotional, educational, and scientific materials through appropriate review processes, ensuring scientific accuracy and compliance. • Contribute to publication strategy, evidence-generation initiatives, investigator-sponsored research review, and real-world evidence activities in collaboration with internal stakeholders. • Support strategic planning and execution for major medical congresses, including content development, stakeholder engagement planning, and insight collection. • Manage complex cross-functional projects, timelines, budgets, and external agency relationships to ensure effective execution of Medical Affairs priorities.

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Source: Employer career site (Workday) First seen: 2026-10-08 Last confirmed: 2026-10-08 How our data works → Report this job

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