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

📌 Drug Safety Case Processing Specialist (Kimberley)
🏢 Placements24
📍 Kimberley