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