Pharmacovigilance Pharmacist
Bring your clinical lens to the world of drug safety and reporting.
Key Responsibilities:
- Analyze adverse event reports and clinical trial safety data.
- Prepare regulatory submissions (e.g., MedWatch, PSURs).
- Collaborate with medical affairs and clinical teams to address safety signals.
Qualifications:
- PharmD with strong understanding of pharmacology.
- Prior experience in drug safety or clinical data review is a plus.
- Detail-oriented with excellent written communication.
Why Join Us?
- Remote or hybrid options
- Pharma industry training provided
- Clear career path into global drug safety