Job Summary

Our clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Monitoring team in South Africa. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivalled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you.

We kindly ask to submit applications in English. Entry level associates with research associate or trial assistant-type backgrounds may also be considered.

Responsibilities

Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
Perform source document verification and case report form review;
Perform regulatory document review;
Conduct study drug inventory;
Perform adverse event and serious adverse event reporting and follow-up;
Assess patient recruitment and retention.

Qualifications

Minimum a Bachelor of science in health-related field or equivalent
Minimum of 1-year independent clinical monitoring
Broad knowledge of medical terminology and clinical patient management
Basic knowledge of drug therapy techniques and clinical research methodologies
Comprehensive knowledge of Local Regulations and ICH GCP
Excellent oral and written communication skills
Fluency in English
Great attention to detail
Must hold a valid driver’s license

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Medpace

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Clinical Research Associate