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IQVIA Inc is seeking experienced Senior Clinical Research Associates in the UK for their sponsor-dedicated team. The role involves site monitoring and management, ensuring compliance with study protocols and regulations, and supporting the execution of clinical trials.
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Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP.
Candidates will work with sites to drive and track subject recruitment plans to enhance predictability for project needs.
IQVIA is a leading global provider of clinical research services committed to accelerating the development of innovative medical treatments.
Matching Summary
Match Score: 75
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IQVIA Inc is seeking experienced Senior Clinical Research Associates in the UK for their sponsor-dedicated team. The role involves site monitoring and management, ensuring compliance with study protocols and regulations, and supporting the execution of clinical trials.
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Skills & Requirements
Must-have
Perform site monitoring visits
Apply Good Clinical Practice guidelines
Manage subject recruitment plans
Maintain Trial Master File documentation
Generate and resolve data queries
Nice-to-have
Strong organizational and problem-solving skills
Effective time and financial management
Ability to establish client relationships
Key Requirements
Bachelor's Degree in scientific discipline or health care
At least 2 years of on-site monitoring experience
Good knowledge of GCP and ICH guidelines
Not eligible for UK visa sponsorship
Work Rights
Must have right to work in UK; no visa sponsorship available