Lead adverse event assessment and regulatory reporting as a Remote Pharmacovigilance Specialist supporting drug safety operations across South Africa. Work fully remotely with global teams.

This experienced specialist supports safety surveillance for marketed and investigational pharmaceutical products. Responsibilities include adverse event processing, safety database use, signal detection, and risk management. The work requires regulatory knowledge and careful communication with internal teams and external stakeholders.

Key Responsibilities:
Collect, process, and assess adverse event reports from wide-ranging sources
Report safety cases accurately to authorities and stakeholders
Maintain safety databases and adverse event information
Prepare PSURs, PBRERs, and additional safety documents




Support signal detection and risk management activities

Requirements:
Bachelor's degree in Pharmacy, Nursing, Life Sciences, or related healthcare field
Minimum three years of pharmacovigilance or drug safety experience
Knowledge of FDA, EMA, and ICH pharmacovigilance guidelines
Experience with Argus, ArisG, or similar safety databases
Solid medical terminology, analytical, and case processing skills

Apply pharmacovigilance expertise, regulatory reporting knowledge, and safety database experience to protect patients through work from home.
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📌 Remote Pharmacovigilance Specialist South Africa Kimberley
🏢 Placements24
📍 Kimberley