Study Co-Ordinator
Pronel Personnel
Durban, KwaZulu Natal, ZA
6d ago

An amazing opportunity has come up for a Study Co-Ordinator, who will be responsible for coordinating and directing the project activities of the clinical trial at our research sites.

  • Study administration, including day to day management of study related activities, people management, compilation and analysis of reports and liaison with all key study stakeholders;
  • Conduct or arrange relevant study related training for staff;
  • Prepare and submit regulatory submissions and follow up on responses and approvals with regulatory agencies;
  • Oversight of QC of all study related source documents;
  • Attend international / national conference calls, study meetings, funder and stakeholder engagement;
  • Compilation and submit study progress reports and all other study related documentation;
  • Maintain and update the Investigator Site File

  • Bachelor’s Degree in a Health-related field with Masters degree in Public Health or Basic Science preferable;
  • At least 3 years’ experience in a similar role within a research environment;
  • SAHPRA, BREC and other regulatory submission experience;
  • Sound knowledge of HIV / AIDS and / or TB research;
  • Understanding of Good Clinical Practices

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