Clinical development studies and/or programs: Contributes to and is key member of a high performing Study Delivery Team (SDT) and is a key member of the Clinical Development Team (CDT) Designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of the asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets. Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working in partnership with Clinical Scientists (CS). Conducts medical data review of trial data, including eligibility review. Responsible for site interactions for medical questions and education (including safety management guidelines Responsible for assessment of key safety-related serious adverse events in partnership with GPVE and oversees safety narratives. Fulfills GCP and compliance obligations for clinical conduct and maintains all required training for same Contributes to key Health Authority interactions and advisory board meetings as Clinical Trial Physician Manages Phase 1 - Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to BMS colleagues in drug discovery, labeling, regulatory, outcomes research, and marketing/commercial departments Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Collaborates with CS on protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion criteria and other safety-related clinical considerations); signs off on protocol. Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders (TLs) in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge and design of clinical development studies and programs. Maintains a strong medical/scientific reputation within the disease area. Has in depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Keeps up-to-date in the disease area via attendance at scientific conferences and ongoing review of the literature. Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape Provides ongoing medical education in partnership with CS, protocol specific training, to support study team, investigators, and others. MD required (or x-US equivalent) functional assignment as Clinical Trial Physician 3 or more years Industry experience with clinical trials required Subspecialty training in oncology and/or hematology or applicable therapeutic area Expertise in using the scientific method to test hypotheses, including statistical design, analysis, and interpretation Knowledge of the drug development process Knowledge of the components needed for an effective clinical plan and protocols Strong leadership skills with proven ability to lead and work effectively in a team environment Ability to present clearly in scientific and clinical settings