Clinical Research Associate, South West England
IQVIA · Bath, UK +1 more
Clinical OperationsFull-timeCompany career page
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Role summary
IQVIA seeks experienced Clinical Research Associates for its sponsor-dedicated team in South West England. The role involves conducting site monitoring visits, managing study progress, and ensuring protocol compliance across interventional clinical trials.
What they're looking for
- Minimum 2 years independent on-site monitoring experience in interventional studies
- Experience across study phases: start-up, enrollment, maintenance, and close-out
- Degree in scientific or healthcare discipline, or equivalent industry experience
- Proficiency with GCP and ICH regulatory guidelines
- Digital literacy and comfort using AI tools professionally
- Strong relationship-building and communication skills
- Full UK right to work; visa sponsorship not available
What you'll be doing
- Conduct site monitoring visits including selection, initiation, monitoring, and close-out activities per GCP/ICH standards
- Collaborate with sites to develop and track recruitment plans aligned with project timelines
- Deliver protocol training and maintain regular site communication to manage expectations
- Assess site compliance with protocol and regulatory requirements; escalate quality issues as needed
- Track study progress including regulatory submissions, enrollment, CRF completion, and data queries
Privacy & handoff
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