Clinical Trial Physician, Neuropsychiatry

Clinical Trial Physician (CTP) Position Summary / Objective Serves as a primary source of medical accountability and oversight for clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1–Phase 3 studies, with demonstrated decision-making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT) Conducts medical data review of trial data, including eligibility review Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines) Assesses 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 (input on inclusion/exclusion and other safety-related clinical considerations) Fulfills GCP and compliance obligations for clinical conduct and maintains all required training Clinical Development Expertise & Strategy Designs and develops clinical plans and protocols with a strategic focus to meet regulatory and disease strategy targets Provides oversight and medical accountability for a group of studies Leads benefit/risk analysis for clinical development protocols in a matrix team environment with Clinical Scientists Partners with CS to support executional delivery of studies (e.g., site activation, enrollment status, adjudication for protocol violations and significant/non-significant deviations) Builds relationships with principal investigators and cultivates thought leaders to gain input on emerging science and program/design of clinical development studies Maintains in-depth disease-area knowledge (etiology, natural history, diagnosis, treatment) and stays current via conferences and literature review Tracks development and regulatory issues related to competitive/relevant compounds and how the portfolio fits the competitive landscape Provides ongoing medical education in partnership with CS to support protocol-specific training Health Authority Interactions & Publications Contributes to key Health Authority interactions and advisory board meetings Authors/drafts clinical content for CSRs, regulatory reports, briefing books, and submission documents (supporting closure, clinical narratives, reporting, and study completion) Degree Requirements MD required (or x-US equivalent) Experience Requirements 3 or more years of industry experience and/or clinical trials experience required Key Competency Requirements Ability to communicate and present information clearly in scientific and clinical settings Subspecialty training in applicable therapeutic area desired Expertise in the scientific method (including statistical design, analysis, and interpretation) Knowledge of the drug development process Knowledge of components needed to execute an effective clinical plan and protocols Strong leadership skills; proven ability to lead and work effectively in a team environment Travel Required Domestic and international travel may be required Compensation & Benefits (as stated) Starting compensation ranges listed by location; additional incentive cash and stock opportunities may be available (based on eligibility) Health coverage Wellbeing support programs Financial wellbeing and protection benefits Paid Time Off (details vary by employee type/location) #J-18808-Ljbffr Scorpion Therapeutics