IQVIA in the United Kingdom is seeking experienced Clinical Research Associates to perform site monitoring visits in accordance with regulatory requirements.
The role involves managing studies, tracking submissions and ensuring compliance with GCP and ICH guidelines. Candidates should have at least 1 year of independent monitoring experience in the UK and possess the ability to establish effective working relationships.
Please note that this position is not eligible for UK visa sponsorship.
#J-18808-Ljbffr