Listed on IQVIA’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role involves reviewing drug safety data across clinical trials and post-market settings, leading signal detection efforts, and preparing regulatory submissions for multiple regions. It suits physicians or clinical professionals transitioning into pharmaceutical safety with several years of industry experience who can synthesize complex data and communicate findings to internal and external stakeholders.
Our summary, not IQVIA’s wording. The full posting is on their site.
What they ask for
Required
- Medical degree from accredited, internationally recognized medical school
- Approximately three years of clinical practice experience plus two years in pharmaceutical or associated industry (or equivalent combination)
- Knowledge of applicable federal and local regulations pertaining to clinical research, safety, and good clinical practice
- Knowledge of assigned product portfolio and therapeutic area
- Experience in signal detection, aggregate reports, and risk management
- Ability to synthesize and critically analyze data from multiple sources
- Strong written and oral communication skills for complex clinical issues
Nice to have
- Mentorship capability