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

Apply to Pharmacovigilance & Drug Safety Specialist (PharmD)