Role Overview



We are seeking an experienced Clinical Research Associate to support clinical trial monitoring, site oversight, and regulatory compliance.



Key Responsibilities



Monitor clinical trial sites for compliance and protocol adherence

Conduct site initiation, monitoring, and close-out visits

Ensure accurate data collection and source documentation

Maintain regulatory documentation and reporting

Support investigator training and site readiness

Ensure adherence to GCP and study protocols



Requirements

Degree in Health Sciences or related field 3+ years CRA experience

Strong understanding of GCP and clinical trial processes

Experience with monitoring and regulatory documentation

Strong organizational and communication skills



Afro-REACH CRO is an equal opportunity employer committed to advancing health equity across SubSaharan Africa.<...