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.

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📌 Senior Clinical Research Associate Kimberley (British Columbia)
🏢 Placements24
📍 British Columbia