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.

REQUIREMENTS

• Experience of independent on-site monitoring in the UK
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility to travel to sites as required
  Apply today and forge a career with greater purpose, make an impact, and never stop learning!

RESPONSIBILITIES

• Site management and monitoring (site selection, site initiation, routine monitoring and close-out visits) in partnership with a single-sponsor
• Working with sites to adapt, drive and track subject recruitment plan
• Providing protocol and study training to assigned sites
• Creating and maintain monitoring visit reports and action plans
• If appropriate, co-monitoring, training and mentoring junior members of the team

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.co