Lead site monitoring and trial documentation as a Senior Clinical Research Associate supporting pharmaceutical studies from Kimberley, Northern Cape.
This senior clinical operations position focuses on investigator-site oversight, protocol adherence, and reliable clinical trial documentation. You will verify source data, prepare monitoring reports, and identify risks for relevant stakeholders. Work includes hybrid administrative responsibilities and required travel.
Key Responsibilities:
- Prepare and present timely monitoring visit reports
- Manage investigational product accountability and dispensing records
- Oversee site readiness and study-specific training
- Identify risks, issues, and discrepancies for escalation
- Participate in study team meetings
Requirements:
- Bachelor's degree in Nursing, Pharmacy, Life Sciences, or related field
- At least four years of CRA experience
- Thorough clinical trial process understanding
- Robust organizational and problem-solving skills
- Ability to travel to investigator sites
Bring monitoring, reporting, and investigational product accountability experience to clinical trials managed from Kimberley.