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Regulatory Affairs Professional

3 weeks ago

Pretoria, Gauteng, South Africa Findojobs-Za Full time

We are seeking a highly skilled Regulatory Affairs Professional to join our team at Findojobs-Za. As a key member of our regulatory affairs department, you will be responsible for ensuring compliance with domestic and international regulations, developing and implementing quality control procedures, and providing expert medical reviews.

Key Responsibilities:
  • Ensure compliance with domestic and international regulations related to clinical trials.
  • Develop and implement quality control procedures to ensure accuracy and reliability of medical information.
  • Collaborate with cross-functional teams to develop and implement data review strategies.
  • Provide expert medical reviews of individual adverse event reports and aggregate case analysis.
Requirements:
  • Medical degree (MD or equivalent), or PharmD.
  • Experience as a clinical scientist who is responsible for timely assessment of the clinical trial data and participation in safety surveillance activities.
  • Excellent knowledge of medical terminology, clinical pharmacology, and regulatory guidelines.
  • Ability to understand clinical data and write clear, concise scientific reports.