Senior Clinical Research Associate – On-Site Monitoring Leader

A leading global clinical research firm in the UK is seeking an experienced Clinical Research Associate to conduct site monitoring and manage clinical trial protocols. Responsibilities include performing monitoring visits, driving subject recruitment, and ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Candidates should have at least 18 months of independent monitoring experience and a life science degree. This role offers career development opportunities in a dynamic environment.#J-18808-Ljbffr…