Director, Global Clinical Physician - Late Oncology
Bristol Myers Squibb
5 days ago
Remote friendly (Lawrence, NJ)
United States
Clinical Research and Development
Position Summary / Objective
- Primary source of medical accountability and oversight for multiple clinical trials
- Matrix management across internal and external network
Position Responsibilities
- Medical Monitoring: contribute to and serve on Study Delivery Team (SDT) and may be on Clinical Development Team (CDT)
- Lead medical data review (including eligibility review)
- Oversee site interactions for medical questions/education (including safety management guidelines)
- Assess key safety-related serious adverse events; oversee safety narratives (with Worldwide Patient Safety)
- Collaborate on protocol input and provide medical strategic oversight (incl. inclusion/exclusion and safety considerations)
- Fulfill GCP and compliance obligations; maintain required training
- Clinical Development Expertise & Strategy: design/develop clinical plans and protocols to meet regulatory/disease strategy targets
- Provide oversight/accountability for a group of studies; lead benefit/risk analysis
- Support study execution (site activation/enrollment status; adjudication for protocol violations and deviations)
- Build relationships with principal investigators and cultivate thought leaders
- Maintain therapeutic area expertise (conferences/literature)
- Provide ongoing medical education to study team/investigators
- Health Authority interactions & publications: medical point of expertise; contribute to CSRs/regulatory reports/briefing books/submission documents
Degree Requirements
- MD required (or x-US equivalent)
Experience/Skills
- 5+ years industry and/or clinical trials experience
- Clear communication; lead presentations
- Subspecialty training in applicable therapeutic area (desired)
- Expertise in scientific method (incl. statistical design/analysis/interpretation)
- Expertise in drug development process and executing clinical plans/protocols
- Strong leadership and teamwork
Travel
- Domestic and international travel may be required.
Compensation/Benefits (as stated)
- Compensation range (Cambridge Crossing): $308,700–$374,075; (Madison/Giralda & Princeton, NJ): $275,630–$333,998. Additional incentives may be available.
- Benefits include medical/dental/vision, wellbeing support, 401(k), disability/life insurance, and other protections.
Work-life
- Paid time off (flexible time off for US exempt; annual vacation/hybrid holiday structure by location/role), plus other eligible leave options.
- Primary source of medical accountability and oversight for multiple clinical trials
- Matrix management across internal and external network
Position Responsibilities
- Medical Monitoring: contribute to and serve on Study Delivery Team (SDT) and may be on Clinical Development Team (CDT)
- Lead medical data review (including eligibility review)
- Oversee site interactions for medical questions/education (including safety management guidelines)
- Assess key safety-related serious adverse events; oversee safety narratives (with Worldwide Patient Safety)
- Collaborate on protocol input and provide medical strategic oversight (incl. inclusion/exclusion and safety considerations)
- Fulfill GCP and compliance obligations; maintain required training
- Clinical Development Expertise & Strategy: design/develop clinical plans and protocols to meet regulatory/disease strategy targets
- Provide oversight/accountability for a group of studies; lead benefit/risk analysis
- Support study execution (site activation/enrollment status; adjudication for protocol violations and deviations)
- Build relationships with principal investigators and cultivate thought leaders
- Maintain therapeutic area expertise (conferences/literature)
- Provide ongoing medical education to study team/investigators
- Health Authority interactions & publications: medical point of expertise; contribute to CSRs/regulatory reports/briefing books/submission documents
Degree Requirements
- MD required (or x-US equivalent)
Experience/Skills
- 5+ years industry and/or clinical trials experience
- Clear communication; lead presentations
- Subspecialty training in applicable therapeutic area (desired)
- Expertise in scientific method (incl. statistical design/analysis/interpretation)
- Expertise in drug development process and executing clinical plans/protocols
- Strong leadership and teamwork
Travel
- Domestic and international travel may be required.
Compensation/Benefits (as stated)
- Compensation range (Cambridge Crossing): $308,700–$374,075; (Madison/Giralda & Princeton, NJ): $275,630–$333,998. Additional incentives may be available.
- Benefits include medical/dental/vision, wellbeing support, 401(k), disability/life insurance, and other protections.
Work-life
- Paid time off (flexible time off for US exempt; annual vacation/hybrid holiday structure by location/role), plus other eligible leave options.