- Hybrid
- Full-time · Mid
- 2–3 years
Serve as a safety and efficacy specialist in a global pharmacovigilance environment by supporting Pharma Research and Development activities with a focus on structured analysis of safety data and documentation.
Responsibilities
- Support end to end pharmacovigilance activities by performing safety data review documentation and validation
- Perform timely case intake data entry and reconciliation activities in safety systems
- Coordinate with cross functional teams in clinical regulatory and medical domains
- Execute routine safety database queries and prepare structured outputs
- Maintain detailed documentation of case processing decisions
Requirements
- Bachelor's degree in a related field
- Nice to have: Pharmacovigilance Professional program
- Nice to have: drug safety credentials
- Nice to have: industry safety training