Associate Director, Global Clinical Physician - Neuropsychiatry

Responsibilities Serves as a primary source of medical accountability and oversight for clinical trials Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Provides ongoing medical education in partnership with CS to allow for protocol-specific training, supporting the study team, investigators, and others Contributes to key Health Authority interactions and advisory board meetings as Associate Director, Global Medical Monitoring Conducts medical data review of trial data, including eligibility review Holds responsibility for site interactions in partnership with the Global Clinical Scientist (CS) for medical questions and education (including safety management guidelines) Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives Collaborates with CS and inputs into protocols, providing medical strategic oversight in protocol development Requirements MD required (or x-US equivalent) 3 or more years of Industry experience and/or clinical trials experience is required Ability to communicate and present information clearly in scientific and clinical settings Subspecialty training in applicable therapeutic area desired Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation Knowledge of drug development process Knowledge of the components needed to execute an effective clinical plan and protocols Strong leadership skills with proven ability to lead and work effectively in a team environment. Core Competencies Demonstrates expertise in medical accountability and oversight for clinical trials, with a strong foundation in the drug development process and the ability to lead cross-functional teams effectively. Proficient in medical data review, safety management, and protocol development, ensuring compliance and scientific rigor throughout the clinical trial phases. Highest-signal resume keywords MD Required Clinical Trials Experience Medical Data Review Drug Development Process Knowledge Leadership Skills ATS Optimization Keywords Hard Skills Hard Skills Medical Accountability Clinical Trial Management Statistical Design Data Analysis Protocol Development Soft Skills Communication Skills Team Collaboration Presentation Skills Industry Keywords Phase 1 Studies Phase 2 Studies Phase 3 Studies Safety Management Guidelines Serious Adverse Events #J-18808-Ljbffr Jobtailor