ARC Regulatory in Belfast is seeking a Clinical Research Associate to monitor in vitro diagnostic device clinical sites, ensuring compliance with the study protocol, ICH GCP, and local regulations. The role involves site qualification, initiation, monitoring, and close-out activities, with occasional travel.
You will prepare detailed monitoring reports, manage study data, liaise with ethics committees, and train site study teams.
#J-18808-Ljbffr
Senior Clinical Research Associate IVD Medical Devices in Lisburn 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.
