About the Role
IQVIA is seeking a Clinical Research Associate for its growing UK Site Management multi-sponsor team. Based in Manchester, Greater Manchester, this full-time CRA2 role involves monitoring clinical trial sites in line with the contracted scope of work and regulatory requirements. You will help maintain clinical research standards while developing your career in a team that welcomes both junior and experienced Clinical Research Associates.
Key Responsibilities
- Perform site selection, initiation, monitoring and close-out visits.
- Deliver site monitoring activities in accordance with the contracted scope of work.
- Monitor compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines and applicable regulatory requirements.
- Work with site teams to identify and follow up on issues arising during monitoring visits.
- Maintain clear records of monitoring activities, findings and follow-up actions.
What You'll Need
- Clinical research knowledge and experience relevant to a Clinical Research Associate role.
- An understanding of GCP, ICH guidelines and regulatory requirements for clinical trials.
- Familiarity with site monitoring activities across the clinical trial lifecycle.
- Strong attention to detail and an organised approach to managing monitoring tasks.
- Clear communication skills and the ability to work effectively with clinical research site teams.
What's on Offer
- A salary of £43,314.
- A full-time role based in Manchester, Greater Manchester.
- The opportunity to join IQVIA’s growing UK multi-sponsor Site Management team.
- Scope to build your clinical research career and continue learning while contributing to meaningful research.
How to Apply
Apply through this listing to express your interest in the CRA2 role at IQVIA. Highlight your relevant clinical research experience and knowledge of site monitoring standards.