Iqvia
Healthcare
ClinicalResearchAssociate
“Clinical Research Associate at Iqvia. Skills: Site monitoring, Clinical research, Regulatory compliance. Perform site monitoring visits. Track subject recruitment plan”
Industry & Context.
Issue resolution
Full UK right to work
What They're Looking For.
Must Have
6 months independent on-site monitoring experience, Experience across start-up, enrolment, maintenance, close-out, Degree in scientific discipline / health care, Equivalent industry experience, Good knowledge of GCP and ICH guidelines, Ability to establish and maintain effective working relationships, Full UK right to work
Nice to Have
AI tools in a professional setting confidence
What You'll Do.
Perform site monitoring visits
Track subject recruitment plan
Administer protocol and study training
Establish communication with sites
Evaluate quality and integrity of study site practices
Escalate quality issues
Manage study progress
Track regulatory submissions and approvals
Track recruitment and enrollment
Track CRF completion and submission
Track data query generation and resolution
Support start-up phase
Ensure site documents are available for filing
Verify Investigator's Site File maintenance
Create documentation regarding site management
Submit regular visit reports
Generate follow-up letters
Collaborate with study team members
How You'll Work.
Team & Collaboration
Study team members
Process & Methodology
Project execution
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