Bristol Myers Squibb
Healthcare
AssociateDirector,GlobalClinicalPhysician-Neuroscience
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“Associate Director, Global Clinical Physician - Neuroscience at Bristol Myers Squibb. Skills: Clinical Development, Medical Monitoring, Protocol Development. Serve as primary source of medical accountability. Provide medical oversight for clinical trials”
Industry & Context.
Domestic travel, International travel
What They're Looking For.
Must Have
MD required, 3 or more years of Industry experience, 3 or more years of clinical trials experience
Nice to Have
Subspecialty training in applicable therapeutic area desired, GCP and compliance obligations for clinical conduct
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
Partner with Global Clinical Scientist
Address medical questions
Provide medical education
Manage safety guidelines
Assess key safety-related serious adverse events
Oversee safety narratives
Provide medical strategic oversight
Fulfill GCP obligations
Fulfill compliance obligations
Maintain all 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
Partner with CS to support executional delivery
Support site activation
Support enrollment status
Adjudicate protocol violations
Adjudicate significant deviations
Adjudicate non-significant deviations
Identify principal investigators
Build relationships with principal 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 clinical development studies
Gain input on clinical development programs
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 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 closure of study
Support clinical narratives
Support reporting of study
Support filing of study
How You'll Work.
Team & Collaboration
Matrix management responsibilities; Cross-functional BMS colleagues; High performing Study Delivery Team; Clinical Development Team; Matrix team environment
Communication Scope
Communicate 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 Associate Director, 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 Globa
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