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Clinical Research Associate

Remote / Online - Candidates ideally in
South Africa
Listing for: Medpace
Full Time, Remote/Work from Home position
Listed on 2026-01-14
Job specializations:
  • Healthcare
    Clinical Research
Job Description & How to Apply Below

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. 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 a health-related field or equivalent;
  • Minimum of 1‑year independent clinical monitoring experience; entry‑level associates with relevant trial assistant or research associate‑type backgrounds may be considered;
  • 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.
Medpace Overview

Medpace is a full‑service clinical contract research organization (CRO). We provide Phase I‑IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti‑viral and anti‑infective.

Headquartered in Cincinnati, Ohio, we employ more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks
  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
Awards
  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What To Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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Position Requirements
10+ Years work experience
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