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About the Role

Bristol Myers Squibb is seeking a Clinical Trial Physician to join their global Clinical Development organization. This role is crucial for the effective design and execution of drug development, driving clinical development strategy, trial design, execution, and interpretation. The position offers meaningful work, growth opportunities, and a supportive environment focused on innovation and patient impact.

Responsibilities

Serves as a primary source of medical accountability and oversight for multiple clinical trials.
Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities.
Provides medical and scientific expertise to cross-functional BMS colleagues.
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).
Leads medical data review of trial data, including eligibility review.
Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education.
Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives.
Leads collaboration with CS and inputs into protocols, providing medical strategic oversight in protocol development.
Fulfills GCP and compliance obligations for clinical conduct and maintains all required training.
Designs and develops clinical plans and protocols with a strong strategic focus.
Provides oversight and medical accountability for a group of studies.
Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment.
Partners with CS to support executional delivery of studies.
Identifies and builds relationships with principal investigators and cultivates thought leaders.
Maintains a strong medical/scientific reputation within the disease area.
Keeps abreast of development and regulatory issues related to other competitive or relevant compounds.
Provides ongoing medical education in partnership with collaborating Clinical Scientists.
Serves as medical point of expertise in key Health Authority interactions and advisory board meetings.
Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents.

Requirements

5 or more years of clinical trial experience, either in industry or academic setting is required.
Ability to communicate information clearly and lead presentations in scientific and clinical settings.
Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation.
Expertise in drug development process.
Expertise in the components needed to execute an effective clinical plan and protocols.
Strong leadership skills with proven ability to lead and work effectively in a team environment.
Domestic and International travel may be required.

Skills

Medical accountability
Medical oversight
Matrix management
Decision making
Medical expertise
Scientific expertise
Protocol development
Clinical plan development
Benefit/risk analysis
Study execution support
Investigator relationship building
Thought leader engagement
Medical/scientific reputation maintenance
Disease area expertise
Competitive landscape analysis
Medical education
Health Authority interactions
Publication authorship
Communication
Presentation skills
Leadership

Location

Remote

Work Type

Remote-by-design

Experience Level

Senior

Education Level

MD required

Benefits

Opportunities for growth
Supportive environment
Inclusion
Wellbeing
Flexibility
Comprehensive benefits

About the Company

Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.

Equal Opportunity

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.
Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.
Bristol Myers Squibb is Disability Confident – Employer
BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.