Coordinate clinical studies by managing participants, documentation, and compliance.
Overview
**A Day in the Life:**
Participant coordination, data capture, protocol compliance, and audit-ready filing.
A Day in the Life
08:00
Study schedule review and participant follow-ups
10:00
Participant visits and data collection
13:00
Data entry and query resolution
15:30
Regulatory documentation and sponsor updates
Career Path
Study Admin Assistant
0-2
Clinical Research Coordinator
2-6
Senior CRC / Trial Manager
6-10
Clinical Operations Lead
10+
Vital Statistics
Salary Range
R 20,000 - R 55,000