Offer summary
Qualifications:
Bachelor's degree in Life Sciences required, Minimum of 5 years of relevant experience, 3 years of experience in pharmacovigilance, Knowledge of safety regulations (FDA, EMA, etc.), Strong medical and scientific writing skills.
Key responsabilities:
- Lead development of aggregate safety reports
- Coordinate process for aggregate report generation
- Perform signal detection and medical analyses
- Develop and manage risk management plans
- Review literature for safety information inclusion