Iqvia
Healthcare
ClinicalResearchAssociate
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Clinical Research Associate at Iqvia. Skills: Site monitoring, Clinical research, Regulatory compliance. Perform site monitoring visits. Work with sites to adapt recruitment plan”
Industry & Context.
25% travel
What They're Looking For.
Must Have
6 months independent on-site monitoring experience, Experience across start-up, enrolment, maintenance, close-out, Digital literacy, including confidence using AI tools, Degree in scientific discipline / health care or equivalent industry experience, Good knowledge of, and skill in applying, applicable clinical research regulatory requirements, Ability to establish and maintain effective working relationships, Full UK right to work
Nice to Have
AI-powered career advancement experience
What You'll Do.
Perform site monitoring visits
Work with sites to adapt recruitment plan
Administer protocol and related study training
Establish regular lines of communication with sites
Evaluate quality and integrity of study site practices
Escalate quality issues
Manage progress of assigned studies
Track regulatory submissions and approvals
Track recruitment and enrollment
Track case report form completion
Track data query generation and resolution
Support start-up phase
Ensure site documents are available for filing
Verify Investigator's Site File maintenance
Create and maintain documentation regarding site management
Submit regular visit reports
Generate follow-up letters
Collaborate and liaise with study team members
How You'll Work.
Team & Collaboration
Study team members
Full Job Description
**Join IQVIA on our mission to accelerate innovation for a healthier world!** IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South West England. **Why IQVIA?** * Career development opportunities to grow as we grow * AI‑powered career advancement through our internal talent marketplace, Career Connections * Mentorship opportunities across the organisation via Employee Resource Groups * Flexible working to assist work–life balance and professional success * Well‑being support covering your physical, mental, and financial health **Awards** * 2026 "Glassdoor Best Place to Work in the UK" * #1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!) * Brandon Hall Excellence Award for Learning & Development **Responsibilities** * Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines * Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability * Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues * Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase * Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in ac
Applying for this Clinical Research Associate role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Iqvia?
Real rants from real employees. Read before you apply.