**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:** o Serve as a member of the respective Global Medical Affairs Team o Provide medical strategic input on treatment landscape in JAPAC to support registrational programs and product life cycle management o Support evidence generation activities including investigator sponsored studies and real-world data o Enable access to medicines through clear understanding and education of treatment value in partnership with cross-functional stakeholders o Support the development of the medical communication strategy and related activities, e.g., product narrative, scientific platform, core content, publications, medical education, and congresses o Contribute to Amgen's Global Safety and global Benefit/Risk profile of a molecule and ensure communication of the implications to external stakeholders o Facilitate and continue to build Amgen’s role as a science-based, patient-focused partner o Contribute to Advisory Board development and execution **Basic Qualifications** o MD/DO degree from an accredited medical school or PhD/PharmD AND o 5 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** o MD plus accredited fellowship in Oncology or related medical discipline, board certified or board eligible o PhD/PharmD will be considered based on individuals’ profile o 10 + years Medical Affairs experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO) o Experience with pipeline assets, launches or supporting mature brands o Regional experience, overseeing affiliates within a given therapeutic area (TA) o Clinical and disease knowledge base in Oncology diseases, including Hematology, Thoracic, Gastrointestinal (GI)/Gastro-urology (GU), and Solid Tumors o Experience with stakeholder engagement and interactions (e.g., OLs, advocacy groups, payers) o Familiarity with global regulatory organizations, guidelines, and practices o Knowledge of Good Clinical Practices (GCP) and global regulations and guidelines o Knowledge of pharmaceutical product development, product lifecycle, and commercialization processes, including but not limited to, clinical operations, commercial, regulatory, and medical affairs o History of solving problems while exhibiting sound scientific/medical judgment and a balanced, realistic understanding of issues o In-depth understanding of scientific method and clinical applications based on medical, scientific, and practical rationale o Track record of success working with matrixed cross-functional teams