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 on-site 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 employer: Placements24
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