Director, Global Clinical Physician – Neuroscience

• Serve as primary source of medical accountability and oversight for multiple clinical trials
• Manage Phase 1–Phase 3 studies and make study decisions
• Provide medical and scientific expertise to cross‑functional BMS colleagues
• Contribute to Study Delivery Teams and potentially Clinical Development Teams
• Lead medical data review, including eligibility review
• Manage site interactions with Clinical Scientists for medical questions and education
• Assess key safety‑related serious adverse events with Worldwide Patient Safety and oversee safety narratives
• Provide medical strategic oversight in protocol development
• Design and develop clinical plans and protocols with the Clinical Development Lead
• Provide oversight and medical accountability for a group of studies
• Lead benefit/risk analysis for clinical development protocols
• Partner with Clinical Scientists on study execution, site activation, enrollment, and protocol deviations
• Identify and build relationships with principal investigators and thought leaders
• Maintain scientific expertise and reputation in the disease area
• Monitor competitive compounds, development, and regulatory issues
• Provide ongoing medical education and protocol‑specific training
• Contribute to Health Authority interactions and advisory board meetings
• Author or draft clinical content for CSRs, regulatory reports, briefing books, and submission documents

Requirements

• MD required (or x-US equivalent)
• 5 or more years of industry experience and/or clinical trials experience required
• Ability to communicate information clearly and lead presentations in scientific and clinical settings
• Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation
• Expertise in the drug development process
• Expertise in 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
• Subspecialty training in applicable therapeutic area desired
• Fulfill GCP and compliance obligations for clinical conduct and maintain all required training
• Domestic and international travel may be required

Core Competencies

Demonstrates expertise in clinical trial management, medical oversight, and protocol development, with a strong focus on safety assessment and regulatory compliance. Proven ability to lead cross‑functional teams and communicate effectively in scientific and clinical settings.

Highest-signal resume keywords

• MD Required
• 5+ Years Industry Experience
• Clinical Trials Experience
• Expertise in Drug Development Process
• Strong Leadership Skills

Hard Skills

• Medical Accountability
• Clinical Plan Development
• Statistical Design and Analysis
• Safety Narrative Oversight
• Benefit/Risk Analysis
• Protocol Development
• Eligibility Review
• Medical Data Review
• GCP Compliance
• Clinical Content Authoring

Soft Skills

• Clear Communication
• Team Collaboration
• Presentation Skills

Industry Keywords

• Clinical Trials
• Phase 1–Phase 3 Studies
• Health Authority Interactions
• Principal Investigators
• Advisory Board Meetings
• Competitive Compound Monitoring
• Medical Education
• Protocol Deviations
• Therapeutic Area Expertise
• Worldwide Patient Safety