CareerPlan

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

United States - California - Foster CityFull-time$196k–$253k2026-10-07 → 2026-11-11

Core

Lead U.S. Medical Affairs strategy for Multiple Myeloma and emerging cellular therapies, driving scientific exchange, evidence generation, and launch readiness.

Role type

Senior IC Associate Director, Medical Affairs

Builds

Scientific communication platforms, medical content, advisory boards, congress initiatives, and evidence-generation programs.

Domain

Oncology (Multiple Myeloma) / Cellular Therapy / Medical Affairs

Required skills

Medical Affairs strategy, evidence generation, publication planning, medical review processes, launch readiness, clinical data interpretation, stakeholder engagement, project management, budget management, cross-functional collaboration

Preferred skills

Advanced degree (MD/PharmD/PhD), hematology experience, Multiple Myeloma expertise, cellular therapy knowledge, congress planning, KOL engagement, matrixed environment leadership

Technologies

Microsoft Word, PowerPoint, Excel, project management tools

Responsibilities

Lead priority workstreams for U.S. Multiple Myeloma Medical Affairs strategy; Serve as strategic medical partner to Field Medical, Commercial, Market Access, HEOR/RWE, Clinical Development, Regulatory, Safety, and Global Medical Affairs teams; Translate clinical data and competitive intelligence into actionable medical strategies; Support development of scientific communication platforms, core medical content, FAQs, presentations, and field-facing resources; Lead or support advisory boards, expert engagement activities, congress initiatives, symposia, and medical education programs; Partner with Field Medical to drive scientific engagement, insight generation, launch readiness, 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; Contribute to publication strategy, evidence-generation initiatives, investigator-sponsored research review, and real-world evidence activities; Support strategic planning and execution for major medical congresses; Manage complex cross-functional projects, timelines, budgets, and external agency relationships; Identify opportunities to improve operational effectiveness and implement practical solutions; Build and maintain strong relationships with key internal stakeholders and external experts; Uphold highest standards of scientific integrity, ethics, compliance, and patient-centricity.

Seniority

Senior, hands-on IC