Clinical Research Associate (CRA)

Johannesburg / Cape Town

Sponsor Dedicated

Join IQVIA – Shape the Future of Clinical Research

We are looking for an experienced Clinical Research Associate to support and oversee clinical trial sites, ensuring the highest standards of quality, compliance, and patient safety.

What You’ll Do

Conduct site selection, initiation, monitoring, and close-out visits in line with GCP and study requirements.

Support sites with recruitment planning and study training.

Monitor study progress, including regulatory submissions, enrollment, data quality, and query resolution.

Ensure proper maintenance of site files and TMF documentation.

Build strong relationships with site staff and collaborate with the study team.

Contribute to site-level financial oversight and start-up activities (where applicable).

What You Bring

Bachelor’s degree in a scientific or healthcare field (or equivalent experience).

Minimum 2 years of on-site monitoring experience.

Experience in the following therapeutic areas are highly beneficial: Respiratory, Gastro Intestinal, Major Depression.

Strong knowledge of ICH-GCP and clinical research regulations.

Excellent communication, organization, and problem-solving skills.

Proficiency with Microsoft Office and digital tools (laptop, iPhone/iPad).

Ability to work independently and build effective partnerships with sites and colleagues.

Why IQVIA?
Join a global leader driving innovation in clinical research. You’ll work alongside talented teams making a meaningful impact on patient outcomes worldwide.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.