SUMMARY:
An amazing opportunity has come up for a Study Co-Ordinator for a 2 year fixed term contract, who will be responsible for coordinating and directing the project activities of the clinical trial at our research sites.
POSITION INFO:
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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