Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Bristol Myers Squibb

Director, Medical Safety Assessment Physician

Bristol Myers Squibb

Director of Medical Safety Assessment leading safety activities and benefit-risk strategies for BMS compounds. Overseeing clinical documents and safety evaluations in compliance with regulatory standards.

Posted 5/5/2026full-timePrinceton • Massachusetts, New Jersey • 🇺🇸 United StatesLead💰 $255,860 - $347,244 per yearWebsite

About the role

Key responsibilities & impact
  • Lead safety activities and benefit-risk strategies for assigned BMS compounds/ program and chair the product Safety Management Team(s).
  • Oversee, prepare and/or review aggregate safety review documents as well as safety sections of relevant clinical trial documents and regulatory filings.
  • Lead team in the evaluation & management of safety signals emerging from any data source. Develop strategy for signal evaluation and document outcome.
  • Act as the Safety Subject Matter Expert for input to regulatory product labeling.
  • Participate/ provide input at cross-functional labeling team meetings and provide regional safety labeling support.
  • Lead process improvement projects. Assist the MSA Therapeutic Area (TA) Head/Lead in developing and maintaining state-of-the-art PV processes and procedures within BMS R&D and PS.
  • Provide input to R&D publication strategy/ plan & ensure safety input to publications/ presentations.
  • Actively drive safety strategy preparation and Represent PS at Health Authority (HA) and Data Monitoring Committee (DMC) meetings.

Requirements

What you’ll need
  • MD/equivalent required.
  • Postgraduate qualification or experience in psychiatry or neurology preferred.
  • 3+ years in PV or relevant pharmaceutical or biomedical field (eg, Medical, Clinical, Regulatory) is strongly preferred.
  • Understanding of the drug development process.
  • Knowledge of PV and ability to apply knowledge to evaluation of safety concerns and minimization of patient risk throughout the life cycle of a drug product.
  • Proficient ability to leverage the range of available tools to investigate safety concerns, including the science of observational research.
  • Understanding of regulatory requirements for safety assessment and action.
  • Strong scientific analytical reasoning skills.
  • Ability to work on multiple projects in parallel.
  • Excellent attention to detail.
  • Excellent verbal and written communication skills.

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. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
pharmacovigilancesafety signal evaluationregulatory product labelingclinical trial documentationaggregate safety reviewdata monitoringobservational researchdrug development processsafety assessmentrisk minimization
Soft Skills
scientific analytical reasoningattention to detailverbal communicationwritten communicationproject managementcross-functional collaborationleadershipprocess improvementstrategic planningteam management
Certifications
MDpostgraduate qualification in psychiatrypostgraduate qualification in neurology