ARC Regulatory is seeking an experienced Clinical Research Associate 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 visits across Belfast and travel as required.
The successful candidate will bring 5+ years in clinical research, with at least 3 years focused on medical device/IVD trials, expertise in SDV, data integrity and regulatory
#J-18808-Ljbffr
IVD Clinical Research Associate - Travel-Ready Monitor in Newtownabbey 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.
