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Amgen

Makes biotech medicines for serious illnesses

Asset Lead Medical Director - Obesity and Related Conditions

Biology & BiotechConfirmed live in the last 24 hours
Full-timeRemote in USARemote

About the Job

Requirements

  • A doctorate degree and 4 years of Medical Affairs, clinical research, or cardiometabolic science research experience; or a master's degree and 7 years of such experience; or a bachelor's degree and 9 years of such experience.
  • Strong clinical and scientific knowledge of cardiometabolic disease, including obesity and related conditions.
  • Experience in U.S. Medical Affairs within the biopharmaceutical industry, including scientific engagement with relevant clinicians, integrated delivery networks, or payers.
  • Experience developing or implementing medical strategy, evidence-generation plans, real-world evidence, health economics and outcomes research, or access-and-use evidence in a matrixed organization.
  • Knowledge of pharmaceutical product development, lifecycle planning, launch readiness, and collaboration across Clinical Operations, Commercial, Regulatory, Market Access, and Medical Affairs.
  • Experience engaging external experts, professional societies, advocacy organizations, health systems, and payers for scientific exchange and insight generation.
  • Ability to integrate multiple indications, scientific narratives, and stakeholder needs into a clear U.S. Medical strategy.
  • Familiarity with global regulatory organizations, guidelines, and practices, including Good Clinical Practice requirements.
  • Demonstrated success leading through influence and working across matrixed, cross-functional teams.

Responsibilities

  • Lead U.S. Cardiovascular & Metabolic Medical strategy, initially emphasizing chronic weight management launch support and early cardiovascular readiness.
  • Build an integrated, evidence-based cardiovascular and metabolic narrative linking obesity and the broader care continuum.
  • Define U.S. scientific evidence gaps and shape local evidence, real-world evidence, health economics and outcomes research, and Access and Use Evidence Generation priorities in alignment with global plans.
  • Synthesize customer, field, market, and medical insights to inform U.S. Medical, Brand, evidence, and implementation decisions.
  • Develop an early external-engagement plan for cardiologists, heart failure specialists, integrated delivery networks, professional societies, payers, and other priority stakeholders.
  • Partner with Global Medical, Global Development, CfOR, HEOR, Medical Value and Access, and Scientific Communications to translate emerging evidence into U.S. strategy and execution.
  • Lead or support U.S. scientific communications, including the scientific platform, core content, publication implementation, congress plans, and medical education.
  • Support clinical trial activities and data interpretation as a U.S. Medical interface with Global Clinical Development and evidence-generation teams.
  • Lead or support advisory boards, expert panels, and implementation-science initiatives to clarify real-world care pathways, referral patterns, and barriers to appropriate care.
  • Provide medical input into reimbursement, policy, regulatory, label, and promotional-material discussions consistent with governance and evidence.
  • Serve as a medical representative in leadership, governance, launch-readiness, and cross-functional teams; recommend priorities and resource trade-offs for the U.S. Medical plan.
  • Contribute to medical training and field scientific readiness for chronic weight management, obstructive sleep apnea, and evolving cardiovascular and metabolic evidence needs.
  • Support decisions on independent medical education, medical grants, sponsorships, and advocacy activities in accordance with company governance.
  • Ensure Medical activities comply with applicable laws, regulations, policies, and standard operating procedures.
  • Use established planning and performance-management processes to measure progress, identify risks, and improve execution.

Desired Qualifications

  • A PharmD, PhD, MD, or other advanced scientific or clinical degree with experience in cardiometabolic disease, obesity, cardiovascular disease, heart failure, or related conditions.
  • Sound judgment and a track record of solving complex cross-functional problems.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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