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 varied 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
- Strong 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