ARC Regulatory is seeking a Clinical Research Associate (CRA) in Belfast to monitor in vitro diagnostic clinical study sites, ensuring compliance with the study protocol, ICH GCP, and local regulations. The role involves site qualification, initiation, monitoring, and close-out activities, with travel as required.
You will work with project leads, coordinate training, conduct SDV and data verification, and liaise with ethics committees.
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IVD Clinical Research Associate — Travel‑Ready Trial Monitor employer: ARC Regulatory
As a leading employer in the clinical research field, we offer a dynamic work environment in Belfast that fosters professional growth and development. Our commitment to employee training ensures that you will receive comprehensive support as you transition into the Research Associate role, while our inclusive culture promotes collaboration and innovation. With opportunities for travel and engagement with diverse clinical sites, you will play a vital role in advancing medical device research and making a meaningful impact in the healthcare sector.
