Cape Town Clinical Study Coordinator – Data & Compliance

A global clinical research organization in Cape Town is seeking an experienced Study Coordinator to manage clinical research activities. The ideal candidate will have strong skills in project management, regulatory submissions, and data collection within clinical trials. You will work closely with cross-functional teams to ensure compliance with regulatory standards and maintain study systems accurately. This role requires a detail-oriented professional with a Bachelor's degree and 3-5 years of relevant experience.

The position offers a full-time limited-duration contract with immediate start date.
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