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