Pharmacovigilance & Drug Safety Specialist (PharmD)
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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