Global Platform Medical Director, Japac, Gi
2 days ago
**Singapore - Singapore**
**JOB ID**:
R-213527
**LOCATION**:
- Singapore - Singapore
**WORK LOCATION TYPE**:
Flex Commuter / Hybrid
**DATE POSTED**:
May. 16, 2025
**CATEGORY**:
Medical Services
**Job Summary**
Reporting to the Global Oncology Executive Medical Director, the Global Platform Medical Director will lead the development and execution of the 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**:
oServe as a member of the respective Global Medical Affairs Team
oProvide medical strategic input on treatment landscape in JAPAC to support registrational programs and product life cycle management
oSupport evidence generation activities including investigator sponsored studies and real-world data
oEnable access to medicines through clear understanding and education of treatment value in partnership with cross-functional stakeholders
oSupport the development of the medical communication strategy and related activities, e.g., product narrative, scientific platform, core content, publications, medical education, and congresses
oContribute to Amgen's Global Safety and global Benefit/Risk profile of a molecule and ensure communication of the implications to external stakeholders
oFacilitate and continue to build Amgen’s role as a science-based, patient-focused partner
oContribute to Advisory Board development and execution
**Basic Qualifications**
oMD/DO degree from an accredited medical school or PhD/PharmD AND
o5 or more years of medical affairs experiences and/or clinical research experience and/or basic science research in Oncology or related medical discipline
**Preferred Qualifications**
oMD plus accredited fellowship in Oncology or related medical discipline, board certified or board eligible
oPhD/PharmD will be considered based on individuals’ profile
o10 + years Medical Affairs experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO)
oExperience with pipeline assets, launches or supporting mature brands
oRegional experience, overseeing affiliates within a given therapeutic area (TA)
oClinical and disease knowledge base in Oncology diseases, including Hematology, Thoracic, Gastrointestinal (GI)/Gastro-urology (GU), and Solid Tumors
oExperience with stakeholder engagement and interactions (e.g., OLs, advocacy groups, payers)
oFamiliarity with global regulatory organizations, guidelines, and practices
oKnowledge of Good Clinical Practices (GCP) and global regulations and guidelines
oKnowledge of pharmaceutical product development, product lifecycle, and commercialization processes, including but not limited to, clinical operations, commercial, regulatory, and medical affairs
oHistory of solving problems while exhibiting sound scientific/medical judgment and a balanced, realistic understanding of issues
oTrack record of success working with matrixed cross-functional teams
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