Global Platform Medical Director, JAPAC, GI
4 days ago
Join to apply for the Global Platform Medical Director, JAPAC, GI role at Amgen
Job SummaryReporting to the Global Oncology Executive Medical Director, the Global Platform Medical Director will lead the development and execution of medical affairs activities and provide medical support to gastrointestinal (GI) cancer assets in collaboration with respective Global Medical Affairs Leads (GMALs) and cross-functional partners.
Responsibilities- Serve as a member of the respective Global Medical Affairs Team
- Provide medical strategic input on the treatment landscape in JAPAC to support registrational programs and product lifecycle management
- Support evidence generation activities including investigator-sponsored studies and real-world data
- Enable access to medicines through understanding and education of treatment value in partnership with cross-functional stakeholders
- Support the development of medical communication strategies and related activities, e.g., product narrative, scientific platform, core content, publications, medical education, and congresses
- Contribute to Amgen's global safety and benefit/risk profile of molecules and communicate implications to external stakeholders
- Build and facilitate Amgen’s role as a science-based, patient-focused partner
- Contribute to advisory board development and execution
- MD/DO degree from an accredited medical school or PhD/PharmD
- At least 5 years of medical affairs, clinical research, or basic science research experience in Oncology or related disciplines
- MD with accredited fellowship in Oncology or related field, board certified or eligible
- PhD/PharmD considered based on profile
- Over 10 years of Medical Affairs experience in the biopharmaceutical industry
- Experience with pipeline assets, launches, or supporting mature brands
- Regional experience overseeing affiliates within a therapeutic area
- Deep knowledge in Oncology diseases, including Hematology, Thoracic, GI/GU, and Solid Tumors
- Stakeholder engagement experience (OLs, advocacy groups, payers)
- Familiarity with global regulatory organizations, guidelines, and practices
- Knowledge of GCP, regulations, and pharmaceutical development processes
- Proven problem-solving skills with sound scientific/medical judgment
- Strong understanding of scientific methods and clinical applications
- Successful track record working with cross-functional teams
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