Job Description: Ensuring compliance with ethics (HREC) regulatory requirements, GCP, standard operating procedures (SOPs), and sponsor requirements; Job Responsibilities: Formative data collecton (e.g., headcounts and focus group discussions); participant recruitment and enrolment; Specimen collection and storage; Overseeing study implementation across four health facilities within study timelines as per protocol requirements: Producing satisfactory regulatory and other required reports and associated documentation in accordance with timelines, SOPs and study-specific requirements; Job Requirements: A nursing, medical, science (or related field) tertiary qualification; Experience in project management, preferably within a research environment; The ability to work accurately according to procedures, rules and regulations; Active registration with the SANC / HPCSA (if applicable); Experience in clinical or operational research;
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