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Study Co-Ordinator
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Study Co-ordinator ? 2-Year Fixed Term Contract Location: Durban Job Description: An established, globally recognised research organisation based in Durban is seeking a Study Co-ordinator to support clinical trial activities. The organisation conducts cutting-edge research in HIV, TB, and COVID-19 across multiple clinical research sites in KwaZulu-Natal. The successful candidate will be responsible for coordinating and managing Phase 1 and 2 clinical trial activities at the eThekwini Clinical Research Site, ensuring studies are conducted efficiently and in compliance with regulatory standards. Minimum Requirements: Bachelor?s Degree in a health-related field Honours, Master?s, or PhD in Public Health or Basic/Clinical Science advantageous Minimum 3 years? experience in a similar role within a research environment Clinical trial experience (involvement in or management of at least one trial) Experience with protocol writing and preparation of study documentation (SOPs, CRFs, LRFs) Experience with regulatory submissions (e.g. SAHPRA, BREC) Strong knowledge of HIV/AIDS and/or TB research Sound understanding of Good Clinical Practice (GCP) and clinical trial processes Leadership and people management experience Strong research focus; publication record advantageous Key Responsibilities: Oversee study administration, including daily operations, team management, reporting, and stakeholder engagement Coordinate and facilitate study-related training for staff Prepare and submit regulatory documentation and manage approval processes Ensure quality control of all study-related documentation Participate in meetings, conference calls, and stakeholder engagements Compile and submit study progress reports and related documentation Maintain and update the Investigator Site File If you meet the above requirements and are looking to contribute to impactful research, we encourage you to apply. .. |
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