Medical Job in Hyderabad – Associate Director at Bristol Myers Squibb
Looking for a rewarding medical job in Hyderabad that makes a global impact? Join Bristol Myers Squibb, a world-renowned biopharmaceutical leader, as an Associate Director, Medical Safety Assessment Physician. This exciting physician job in Hyderabad allows you to lead safety strategy, evaluate benefit-risk profiles, and shape the future of patient safety worldwide. If you’re seeking a meaningful associate director job in a company that values innovation, collaboration, and purpose, this opportunity is made for you.
Job Details:
- Job Position: Associate Director, Medical Safety Assessment Physician
- Location: Hyderabad, Telangana, India
About the Company
Bristol Myers Squibb (BMS) is a global leader in biopharmaceutical innovation, transforming lives through science. Known for its inclusive culture and commitment to excellence, BMS provides professionals with the opportunity to work on cutting-edge research, from immunology to oncology. Employees enjoy flexibility, continuous learning, and a purpose-driven work environment.
Medical Job in Hyderabad – Qualifications & Experience
- Education: MD or equivalent qualification (postgraduate in Internal Medicine, Immunology, Oncology, or related specialty preferred).
- Experience: Minimum 3 years in Pharmacovigilance or related biomedical, regulatory, or clinical fields.
Job Description
This associate director job offers you the chance to lead global medical safety initiatives for Bristol Myers Squibb’s innovative portfolio. As part of the Worldwide Patient Safety (WWPS) team, you’ll develop benefit-risk strategies, oversee safety documentation, and ensure compliance with international regulatory standards. This is a prestigious medical job in Hyderabad for those who want to blend clinical expertise with leadership in pharmacovigilance and drug safety.
Key Responsibilities
- Lead safety activities and benefit-risk strategies for assigned BMS compounds and programs.
- Chair product Safety Management Teams and ensure regulatory compliance.
- Oversee and review aggregate safety documents such as DSURs, PBRERs, and CSRs.
- Manage emerging safety signals from clinical and post-marketing data sources.
- Lead and support safety labeling activities and regulatory submissions.
- Guide process improvement projects and advance pharmacovigilance (PV) standards.
- Provide input to R&D publication plans and contribute to scientific presentations.
- Represent BMS at regulatory, advisory, and Data Monitoring Committee meetings.
- Mentor colleagues, promote teamwork, and ensure operational excellence.
Clinical Development Responsibilities
- Act as global safety lead for compounds in clinical development.
- Provide safety input to clinical study designs, protocols, and amendments.
- Support integrated safety summaries and pre-submission documentation.
- Develop safety-focused content for advisory and regulatory interactions.
Post-Marketing Support
- Lead post-marketing safety initiatives and ensure compliance with global safety standards.
- Evaluate post-market safety signals and prepare Safety Topic Reviews.
- Oversee risk management plans (RMPs) and ensure labeling reflects real-world safety data.
- Collaborate with epidemiology and medical affairs on post-marketing safety studies.
Department & Cross-Functional Activities
- Drive safety process optimization and ensure audit readiness.
- Partner with cross-functional teams—Legal, Operations, and Marketing-to maintain safety integrity.
- Provide internal training on product safety and pharmacovigilance best practices.
- Support manufacturing quality initiatives and integrated health hazard assessments.
Medical Job in Hyderabad – Skills & Competencies:
- In-depth understanding of drug development and safety evaluation.
- Knowledge of global pharmacovigilance regulations.
- Strong analytical, leadership, and communication skills.
- Ability to manage multiple international projects effectively.
