Director, Global Clinical Physician – Late Oncology

Bristol Myers Squibb

Director overseeing clinical trials at Bristol Myers Squibb, responsible for medical accountability and leading clinical strategies. Focusing on drug development in a cross-functional team environment.

Posted 5/27/2026full-timePrinceton • Massachusetts, New Jersey • 🇺🇸 United StatesLead💰 $275,630 - $374,075 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Serves as a primary source of medical accountability and oversight for multiple clinical trials
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 other GCPs and Global Clinical Scientists (GCSs) for medical questions and education (including safety management guidelines)
Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives
Leads collaboration with GCS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations)
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 based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets
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 working with other GCPs and Global Clinical Scientists (GCSs)

Requirements

What you’ll need

MD required (or x-US equivalent)
5 or more years of Industry experience and/or clinical trials experience is required
Ability to communicate information clearly and lead presentations in scientific and clinical settings
Subspecialty training in applicable therapeutic area desired
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.

Benefits

Comp & perks

Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trialsmedical data reviewsafety management guidelinesprotocol developmentbenefit/risk analysisstatistical designdata analysisdrug development processclinical plan execution

Soft Skills

communicationleadershipteam collaborationpresentation skills

Certifications