Oversee clinical trials as a Senior Clinical Research Associate in hybrid Kimberley, applying site monitoring expertise and Good Clinical Practice knowledge.

This experienced Senior Clinical Research Associate supports clinical operations within a pharmaceutical company advancing patient care through research. You will manage investigator-site activities, maintain trial data integrity, and support clinical development programs. The position combines in office visits with remote administrative work.

Key Responsibilities:

- Conduct site initiation, monitoring, and close-out visits
- Verify source documents against case report forms
- Monitor subject recruitment and retention efforts
- Ensure regulatory, GCP, and protocol compliance
- Build investigator and site staff relationships

Requirements:

- Bachelor's degree in Life Sciences or related healthcare field
- Minimum four years as a Clinical Research Associate
- Understanding of ICH-GCP and regulatory requirements
- Experience conducting and documenting monitoring visits
- Proficiency with CTMS and EDC systems

Apply clinical trial oversight, site monitoring, and GCP expertise across investigator sites in Kimberley, Northern Cape.

📌 Senior Clinical Research Associate Kimberley
🏢 Placements24
📍 Kimberley