CRA2 - Multi-Sponor Department

IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.



Apply today and forge a career with greater purpose, make an impact, and never stop learning!



**Responsibilities**



+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability

+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues

+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence...