Iqvia
Healthcare
ClinicalResearchAssociateII
Neural analysis suggests this role is
optimal for Mid candidates.
“Clinical Research Associate II at Iqvia. Skills: Site monitoring, Clinical research, Regulatory compliance. Perform site monitoring visits. Adapt, drive, and track subject recruitment plan”
Industry & Context.
Access to vehicle required for travel
What They're Looking For.
Must Have
2 years on-site monitoring experience, Degree in scientific discipline / health care or equivalent industry experience, Good knowledge of GCP and ICH guidelines, Full driving license and access to vehicle
What You'll Do.
Perform site monitoring visits
and track subject 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
Support start-up phase
Ensure site documents are available for filing
Verify Investigator's Site File is maintained
Create and maintain documentation
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’s Site Management (full service / multi-sponsor) team is growing and seeking experienced Clinical Research Associates in Ireland. **Why IQVIA?** * Genuine 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 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!) - #1 in category * 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 accordance with GCP and local regu
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