Bristol Myers Squibb
Healthcare
Director,GlobalClinicalPhysician
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“Director, Global Clinical Physician at Bristol Myers Squibb. Skills: Clinical trials, Drug development, Medical monitoring, Health authority interactions. Serve as primary source of medical accountability. Provide medical oversight for clinical trials”
Industry & Context.
Decision making capabilities
Domestic travel may be required, International travel may be required
What They're Looking For.
Must Have
3 or more years of Industry experience, 3 or more years of clinical trials experience, MD required
Nice to Have
Subspecialty training in applicable therapeutic area, Expertise in the scientific method, Knowledge of drug development process, Knowledge of components to execute clinical plan, Leadership skills, Ability to work effectively in a team
What You'll Do.
Serve as primary source of medical accountability
Provide medical oversight for clinical trials
Manage Phase 1 – Phase 3 studies
Provide medical and scientific expertise
Conduct medical data review
Hold responsibility for site interactions
Address medical questions
Provide medical education
Manage safety guidelines
Assess serious adverse events
Oversee safety narratives
Collaborate on protocols
Provide medical strategic oversight
Fulfill GCP obligations
Fulfill compliance obligations
Maintain required training
Design clinical plans
Develop clinical plans
Develop clinical protocols
Provide oversight for studies
Provide medical accountability for studies
Lead analysis of benefit/risk
Support executional delivery of studies
Identify principal investigators
Build relationships with investigators
Identify thought leaders
Cultivate thought leaders
Gain input on emerging science
Gain input on drug research
Gain input on biomarker research
Gain input on disease knowledge
Gain input on study design
Gain input on program design
Maintain medical/scientific reputation
Keep up-to-date in disease area
Attend scientific conferences
Review the literature
Keep abreast of development issues
Keep abreast of regulatory issues
Provide ongoing medical education
Provide protocol-specific training
Support the study team
Support investigators
Contribute to Health Authority interactions
Contribute to advisory board meetings
Author clinical content for CSRs
Draft clinical content for CSRs
Author regulatory reports
Draft regulatory reports
Author briefing books
Author submission documents
Draft submission documents
Support study closure
Support clinical narratives
Support study reporting
Support study filling
How You'll Work.
Team & Collaboration
Matrix management responsibilities; Cross-functional BMS colleagues; Study Delivery Team; Clinical Development Team; Matrix team environment
Communication Scope
Communicate information clearly; Present information clearly
Full Job Description
**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: [careers.bms.com/working-with-us](https://careers.bms.com/working-with-us). **Functional Area Description** The Global Clinical Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. **Position Summary / Objective** * Serves as a primary source of medical accountability and oversight for clinical trials * Matrix management responsibilities across the internal and external network * Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities * Provides medical and scientific expertise to cross-functional BMS colleagues **Position Responsibilities** _Medical Monitoring_ * Contributes to and is a key member of a high performing Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT) * Conducts medical data review of trial data, including eligibility review * Holds responsibility for site interactions in partnership with the Global Clinical Scientist
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