CRA Job at IQVIA in the UK | Apply Now
Looking for a CRA job in the UK? IQVIA is hiring a Clinical Research Associate in Reading, United Kingdom. This is an exciting opportunity for professionals in life sciences to work on oncology studies, gain hands-on experience, and grow within one of the leading global CROs. If you’re exploring IQVIA careers or searching for life science jobs in UK, this role could be your perfect next step.
Job Details
- Job Position: Clinical Research Associate (CRA)
- Location: Reading, United Kingdom (Field-based)
- Job ID: R1514135
About the Company
IQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The company focuses on creating intelligent connections that accelerate the development and commercialization of innovative medical treatments. With a strong global presence, IQVIA plays a key role in improving patient outcomes and advancing population health worldwide. For professionals exploring IQVIA careers, the company offers strong learning opportunities and long-term career growth.
Job Description
IQVIA is seeking a Clinical Research Associate to join its Site Management (multi-sponsor) team. This CRA job involves supporting oncology studies and managing clinical trial sites across the UK. The role is field-based and offers the opportunity to work closely with research sites, ensuring compliance with protocols and regulatory standards.
This position is ideal for candidates looking for life science jobs in UK with hands-on monitoring experience and career advancement opportunities.
Qualifications
- Experience in independent on-site monitoring in the Oncology therapeutic area (unblinded studies).
- Strong knowledge of Good Clinical Practice (GCP) and ICH guidelines.
- Life science degree or equivalent industry experience.
- Flexibility to travel across sites in the UK.
Key Responsibilities
- Perform site monitoring visits including selection, initiation, monitoring, and close-out visits in accordance with Good Clinical Practice (GCP).
- Work with sites to adapt, drive, and track subject recruitment plans.
- Administer protocol and study-related training to assigned sites.
- Maintain regular communication with sites to manage expectations and resolve issues.
- Evaluate site practices to ensure adherence to protocols and regulatory requirements.
- Track study progress including regulatory submissions, approvals, and enrollment.
- Ensure proper documentation in Trial Master File (TMF) and Investigator’s Site File (ISF).
- Prepare monitoring visit reports, follow-up letters, and study documentation.
- Collaborate with study teams to support project execution.
