$255,860 – $310,040
Listed on Bristol Myers Squibb’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
Lead medical safety strategy and oversight for assigned pharmaceutical compounds across development and postmarketing phases, managing benefit-risk evaluations and regulatory submissions. Suited for physicians with pharmacovigilance experience who want to direct patient safety strategy at a major pharmaceutical company.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- MD or equivalent medical degree
- Understanding of drug development process
- Knowledge of pharmacovigilance and safety evaluation
- Understanding of regulatory requirements for safety assessment
- Strong scientific and analytical reasoning
- Ability to manage multiple projects in parallel
- Excellent written and verbal communication
Nice to have
- 3+ years in pharmacovigilance or pharmaceutical field
- Postgraduate qualification in internal medicine, immunology, oncology, or related specialty
- Experience in clinical research or observational research
- Experience in clinical practice