Global Platform Medical Director, JAPAC, GI
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Job Summary
Reporting 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
Basic Qualifications
MD / DO degree from an accredited medical school or PhD / PharmDAt least 5 years of medical affairs, clinical research, or basic science research experience in Oncology or related disciplinesPreferred Qualifications
MD with accredited fellowship in Oncology or related field, board certified or eligiblePhD / PharmD considered based on profileOver 10 years of Medical Affairs experience in the biopharmaceutical industryExperience with pipeline assets, launches, or supporting mature brandsRegional experience overseeing affiliates within a therapeutic areaDeep knowledge in Oncology diseases, including Hematology, Thoracic, GI / GU, and Solid TumorsStakeholder engagement experience (OLs, advocacy groups, payers)Familiarity with global regulatory organizations, guidelines, and practicesKnowledge of GCP, regulations, and pharmaceutical development processesProven problem-solving skills with sound scientific / medical judgmentStrong understanding of scientific methods and clinical applicationsSuccessful track record working with cross-functional teamsJ-18808-Ljbffr