Global Asset Lead Medical Director, Prostate Cancer, US – Remote @Amgen

Job Information

Job Description:

What you will do

Let’s do this. Let’s change the world. In this vital role you will be accountable for development and delivery of the global medical affairs strategy for Amgen’s Prostate Cancer portfolio. The Asset Lead Medical Director will also be accountable for the Global Medical Affairs Team (GMAT) with the objective of enhancing Amgen’s value proposition.


  • Lead the cross-functional and cross-regional development of the global medical affairs strategies for Amgen’s Prostate Cancer portfolio through the GMAT
  • Provide support for the development and delivery of the clinical development plan for the prostate cancer portfolio
  • Actively provide insights and support the development of the early Target Product Profile
  • Coordinate with the regions to develop and lead the external stakeholder management plan, communication strategy, scientific platform, publication plan and evidence generation plans for the prostate cancer portfolio
  • Develop robust external stakeholder engagement and insight gathering to strengthen understanding of the unmet need and maximize medical value of the prostate cancer portfolio
  • Enhance Amgen’s reputation as a science-based and patient focused reliable partner
  • Partner on evidence generation and ensure key regional/local needs are addressed

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The medical professional we seek is a leader with these qualifications.

Basic Qualifications:

MD or DO degree from an accredited medical school OR PhD OR PharmD


2 years of clinical research experience and/or basic science research in Hematology-Oncology

Preferred Qualifications:

  • MD plus accredited fellowship in Oncology, board certified or board eligible
  • Clinical and disease knowledge base in prostate cancer
  • 4+ years Hematology or Oncology Medical Affairs experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO) that includes collaborations with integrated delivery networks, accountable care organizations, and/or payers
  • 2+ years of clinical research experience and/or basic science combined with clinical teaching and patient care activities
  • Familiarity with global regulatory organizations, guidelines, and practices
  • Knowledge of Good Clinical Practices (GCP) and global regulations and guidelines
  • History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues
  • Knowledge of pharmaceutical product development, product lifecycle, and commercialization processes, including but not limited to, clinical operations, commercial, regulatory, and medical affairs

Experience Level: Executive
Work From: Remote from Country

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