Responsible for implementation, planning, and execution of assigned clinical trial activities in Early Clinical Development Provides clinical, medical and scientific expertise to cross-functional BMS colleagues Participates in designing and developing clinical studies and research plans in support of asset strategy with the Early Clinical Development Leadership team; clinical studies include first-in-human Phase I, proof of concept Phase I/II, entry registrational studies, biomarker qualification studies, and/or clinical pharmacology studies Liaises with Translational & Discovery Scientists and Development Teams to define dose and schedule, indications, and patient selection (e.g., biomarker qualification and implementation) Provides oversight and medical accountability for multiple trials across early development clinical lifecycle Works on multiple trials across early development clinical lifecycle Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment Maintains a thorough understanding of assigned protocols and protocol requirements and educate team members Manage protocol and ICF development process (e.g., documents and amendments) with minimal guidance; includes writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality in collaboration with Medical Writing. Present to governance committee and early clinical development team meetings as required. Plans and leads the implementation of clinical study startup/conduct/close-out activities as applicable. Manages site interactions for medical questions and education (including safety management guidelines). Develop clinical narrative plan and review clinical narratives. Fulfills GCP and compliance obligations for clinical conduct and maintains all required training Contributes to key Health Authority interactions and advisory board meetings as Early Clinical Development Physician; serves as Primary Clinical Representative in Regulatory interactions for early development projects MD or DM in Clinical Pharmacology or Oncology 10+ years of experience in clinical science, clinical research, or equivalent Medical Monitoring experience in Early Clinical Development is desirable Advanced knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations Proficient in Microsoft Word, Excel, PowerPoint, Electronic Data Capture (e.g., RAVE), J-Review or similar data reporting tools Experience in driving, managing and collaborating in a team/matrix work environment Recognized internally and externally as a Therapeutic Area and Functional expert