Director, Global Clinical Physician - Late Oncology
Bristol Myers Squibb
12 days ago
Remote friendly (Madison, NJ)
United States
Clinical Research and Development
Position Summary / Objective
- Serves as a primary source of medical accountability and oversight for multiple clinical trials.
- Matrix management responsibilities across the internal and external network.
Position Responsibilities
- Contributes to and serves as a key member of a Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT).
- Leads medical data review of trial data, including eligibility review.
- Leads site interactions for medical questions and education (including safety management guidelines) in partnership with GCPs and Global Clinical Scientists (GCSs).
- Assesses key safety-related serious adverse events with Worldwide Patient Safety and oversees safety narratives.
- Collaborates with GCSs and provides medical strategic oversight in protocol development (e.g., inclusion/exclusion and safety considerations).
- Fulfills GCP and compliance obligations for clinical conduct; maintains required training.
- Designs and develops clinical plans and protocols with strategic focus to meet regulatory and disease strategy targets.
- Provides oversight and medical accountability for a group of studies.
- Leads benefit/risk analysis for protocols in a matrix environment.
- Partners with GCPs/GCSs to support study delivery (site activation, enrollment status, adjudication of protocol violations/deviations).
- Builds relationships with principal investigators and thought leaders.
- Maintains deep disease-area scientific expertise; stays current with literature and development/regulatory issues.
- Provides ongoing medical education with Clinical Scientists.
- Serves as medical point of expertise for Health Authority interactions and advisory boards.
- Authors/drafts clinical content for CSRs, regulatory reports, briefing books, and submission documents.
Qualifications
- MD required (or x-US equivalent).
- 5+ years of industry and/or clinical trials experience (required).
Key Competency Requirements
- Clear scientific/clinical communication; ability to lead presentations.
- Subspecialty training in applicable therapeutic area (desired).
- Expertise in scientific method (statistical design, analysis, interpretation).
- Expertise in drug development process and clinical plan/protocol execution.
- Strong leadership and teamwork skills.
Travel
- Domestic and international travel may be required.
Application Instructions
- Apply for the role even if your resume does not perfectly align.
- Serves as a primary source of medical accountability and oversight for multiple clinical trials.
- Matrix management responsibilities across the internal and external network.
Position Responsibilities
- Contributes to and serves as a key member of a Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT).
- Leads medical data review of trial data, including eligibility review.
- Leads site interactions for medical questions and education (including safety management guidelines) in partnership with GCPs and Global Clinical Scientists (GCSs).
- Assesses key safety-related serious adverse events with Worldwide Patient Safety and oversees safety narratives.
- Collaborates with GCSs and provides medical strategic oversight in protocol development (e.g., inclusion/exclusion and safety considerations).
- Fulfills GCP and compliance obligations for clinical conduct; maintains required training.
- Designs and develops clinical plans and protocols with strategic focus to meet regulatory and disease strategy targets.
- Provides oversight and medical accountability for a group of studies.
- Leads benefit/risk analysis for protocols in a matrix environment.
- Partners with GCPs/GCSs to support study delivery (site activation, enrollment status, adjudication of protocol violations/deviations).
- Builds relationships with principal investigators and thought leaders.
- Maintains deep disease-area scientific expertise; stays current with literature and development/regulatory issues.
- Provides ongoing medical education with Clinical Scientists.
- Serves as medical point of expertise for Health Authority interactions and advisory boards.
- Authors/drafts clinical content for CSRs, regulatory reports, briefing books, and submission documents.
Qualifications
- MD required (or x-US equivalent).
- 5+ years of industry and/or clinical trials experience (required).
Key Competency Requirements
- Clear scientific/clinical communication; ability to lead presentations.
- Subspecialty training in applicable therapeutic area (desired).
- Expertise in scientific method (statistical design, analysis, interpretation).
- Expertise in drug development process and clinical plan/protocol execution.
- Strong leadership and teamwork skills.
Travel
- Domestic and international travel may be required.
Application Instructions
- Apply for the role even if your resume does not perfectly align.