Job Description
Pharmacovigilance & Drug Safety Specialist (PharmD)
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
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