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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