Study Coordinator

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;