Bristol Myers Squibb

Healthcare

Director,GlobalClinicalPhysician

$240–360k ~AI est. Switzerland FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Director candidates.

The Brief

“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.

Healthcare
Problems you'll solve

Decision making capabilities

Eligibility Requirements

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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