Director, Global Clinical Physician - Late Oncology Position within Clinical Development dedicated to the effective design and execution of drug development. Position Summary / Objective Primary source of medical accountability and oversight for multiple clinical trials. Matrix management responsibilities across internal and external networks. Position Responsibilities Medical Monitoring Key member of a high performing Study Delivery Team (SDT) and may be member of the Clinical Development Team (CDT). Lead medical data review of trial data, including eligibility review. Responsible for site interactions in partnership with other GCPs and Global Clinical Scientists (GCSs) for medical questions and education. Responsible for assessment of key safety‐related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives. Lead collaboration with GCS and provide inputs into protocols, offering medical strategic oversight in protocol development. Fulfill GCP and compliance obligations for clinical conduct and maintain all required training. Clinical Development Expertise & Strategy Design and develop clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area, and relevant science. Provide oversight and medical accountability for a group of studies. Lead analysis of benefit/risk for clinical development protocols in a matrix team environment. Partner with other GPCs / GCSs to support executional delivery of studies. Identify and build relationships with principal investigators and cultivate thought leaders. Maintain strong medical/scientific reputation within the disease area. Stay abreast of development and regulatory issues related to other competitive or relevant compounds. Provide ongoing medical education in partnership with collaborating Clinical Scientists. Health Authority Interactions & Publications Contribute and serve as medical point of expertise in key Health Authority interactions and advisory board meetings as Director, Global Clinical Physician. Author/draft clinical content for CSRs, regulatory reports, briefing books and submission documents. Degree Requirements MD required (or U.S. equivalent). Experience Requirements 5 or more years of industry experience and/or clinical trials experience is required. Key Competency Requirements 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. Travel Required Domestic and International travel may be required. Compensation Overview Cambridge Crossing: $308,700 - $374,075 Madison - Giralda - NJ - US: $275,630 - $333,998 Princeton - NJ - US: $275,630 - $333,998 Benefits 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. Paid Time Off – US Exempt Employees: flexible time off, 11 paid national holidays. Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non‑Exempt, Hourly Employees: 160 hours annual paid vacation, 11 national holidays, and 3 optional holidays. Location: Cambridge Crossing-MA Req Number: R Equal Employment Opportunity Statement Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. #J-18808-Ljbffr