Description
Join IQVIA on its mission to drive healthcare forward as a Clinical Research Associate in the UK.
IQVIA, a leading global provider of clinical research services, commercial insights, and healthcare intelligence, is seeking experienced Clinical Research Associates.
Why IQVIA?
- Recognized as #1 in its category on the 2026 Fortune World's Most Admired Companies list for the fifth consecutive year
- Genuine career development opportunities
- Work on cutting-edge medicines at the forefront of new medicines development
- Access to significant data pools for better site selection and recruitment
Responsibilities
- Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
- Work with sites to adapt, drive, and track subject recruitment plans
- Administer protocol and related study training to assigned sites
- Evaluate the quality and integrity of study site practices
- Manage the progress of assigned studies
- Ensure site documents are available for filing in the Trial Master File
- Create and maintain documentation regarding site management and monitoring visit findings
- Collaborate with study team members for project execution support
Requirements
- Minimum of 18 months of independent on-site monitoring
- Experience managing multiple clinical trial protocols across diverse investigative sites
- 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
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Please note - this role is not eligible for UK visa sponsorship