IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK to join us on our mission to help create a healthier world.

Responsibilities

Site management and monitoring (site selection, site initiation, routine monitoring and close-out visits) in partnership with a single-sponsorWorking with sites to adapt, drive and track subject recruitment planProviding protocol and study training to assigned sitesCreating and maintain monitoring visit reports and action plansIf appropriate, co-monitoring, training and mentoring junior members of the team  

Requirements

Experience of independent on-site monitoring in the UKIn depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesLife science degree educated or equivalent industry experienceFlexibility to travel to sites as required

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

#LI-ADAMTHOMPSON

*Please note - this role is not eligible for UK visa sponsorship*

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com