Process adverse event cases and maintain safety databases as a Remote Pharmacovigilance Specialist serving pharmaceutical safety operations. Support accurate reporting from South Africa.

This specialist evaluates safety information from clinical trials and post-marketing sources for marketed and investigational products. The position emphasizes case processing, medical terminology, regulatory submissions, and data integrity. You will also review literature, answer safety inquiries, and collaborate across medical, clinical, regulatory, and legal departments.

Key Responsibilities:
Process adverse event reports from clinical and post-marketing sources
Review literature for product-related safety information
Respond to internal and external safety inquiries




Ensure compliance with regulations and company standard operating procedures
Improve pharmacovigilance processes and systems continuously

Requirements:
Three or more years in pharmacovigilance or drug safety
Healthcare-related bachelor's degree; advanced degree advantageous
Experience with adverse event reporting systems and safety databases
Excellent written and verbal communication skills
Independent task management and robust organizational abilities remotely

Use exact case processing, communication, and compliance skills to strengthen adverse event reporting and pharmaceutical safety surveillance.

📌 Drug Safety Case Processing Specialist Kimberley
🏢 Placements24
📍 Kimberley