Director, Global Clinical Trial Physician
Bristol Myers Squibb
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ERGOMED
Posted: 10/19/2026Director, Global Clinical Trial Physician
Bristol Myers SquibbCore Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Development Strategy, including protocol development, regulatory submission, and adherence to GCP/ICH guidelines. Proven ability to lead complex clinical studies and collaborate effectively across global teams while maintaining high scientific and regulatory standards.
Highest-signal resume keywords
Clinical R&D ExperienceGCP/ICH Guidelines KnowledgeProtocol Development ExpertiseScientific Data Review SkillsCross-Functional Collaboration
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Contribute to the Global Clinical Development Strategy for assigned assets and indications
- Serve as subject matter expert for clinical study development, conduct and regulatory submission
- Support protocol development through CSR review and validation
- Contribute to clinical development plans, strategic discussions and harmonisation of standards
- Lead clinical oversight of study data, including CRF interdependencies, data conventions, review tools and visualisations
- Collaborate with Data Management and Programming
- Serve as Trial Lead for complex clinical studies when required
- Present data and insights to investigators, study staff, senior leadership and external stakeholders
- Partner with the CCOE Clinical Capabilities Team on process improvements and departmental training
- Share best practices, communicate lessons learned, and coach and mentor colleagues
Requirements
What you’ll need- Degree in Life Sciences — MD, PhD, PharmD, MS, RN or equivalent scientific discipline
- 10+ years of experience in Clinical R&D, including operating in a matrix environment
- Recognised expertise in the relevant Therapeutic Area and/or Clinical Science function
- Advanced knowledge of GCP/ICH guidelines and the full drug development lifecycle, from discovery through registration
- Strong understanding of study design, statistics, clinical operations and the regulatory environment
- Experience with protocol development, data review, CSR validation and regulatory documentation
- Advanced scientific data review, trend identification, interpretation and reporting skills
- Ability to present complex scientific information clearly to study coordinators, senior leadership, external KOLs and investigators
- Cross-functional collaboration skills in complex global programmes
- Commitment to high scientific and regulatory standards
Benefits
Comp & perks- Opportunities for growth
- Supportive, inclusive environment
- Wellbeing support
- Flexible work arrangements
- Comprehensive benefits
- Reasonable workplace accommodations/adjustments
- Ongoing role support
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Study DevelopmentRegulatory SubmissionData ReviewCSR ValidationStudy DesignStatisticsClinical OperationsTrend IdentificationInterpretation and Reporting
Soft Skills
Presentation SkillsCoaching and MentoringCommunication Skills
Certifications & Qualifications
Degree in Life Sciences
Industry Keywords
Therapeutic Area ExpertiseDrug Development LifecycleMatrix EnvironmentClinical OversightProcess Improvements