Clinical Research Associate

IQVIA

. Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits, in accordance with contracted scope and regulatory requirements .

Posted 9/29/2026full-timeBath • United KingdomJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in site monitoring and management for clinical trials, ensuring compliance with regulatory requirements and effective communication with study sites. Proficient in applying Good Clinical Practice (GCP) and ICH guidelines while managing project execution and documentation.

Highest-signal resume keywords

On-Site Monitoring ExperienceGood Clinical Practice (GCP)International Conference on Harmonization (ICH)Regulatory Submissions TrackingDigital Literacy

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Site MonitoringProtocol AdministrationRegulatory ComplianceData Query ResolutionStudy Start-Up SupportCRF CompletionRecruitment PlanningQuality EvaluationDocumentation ManagementProject Execution

Soft Skills

Effective CommunicationRelationship Management

Tools & Technologies

AI Tools

Industry Keywords

Clinical ResearchInterventional StudiesTrial Master FileInvestigator's Site FileStudy Maintenance

About the role

Key responsibilities & impact

Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits, in accordance with contracted scope and regulatory requirements
Work with sites to adapt, drive, and track subject recruitment plans
Administer protocol and related study training to assigned sites
Establish regular communication with sites to manage project expectations and issues
Evaluate study-site quality and integrity regarding protocol conduct and regulatory adherence; escalate quality issues
Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data-query generation and resolution
Support the study start-up phase as needed
Ensure site documents are available for Trial Master File filing and verify Investigator's Site File maintenance
Create and maintain site-management and monitoring documentation, including visit reports and follow-up letters
Collaborate with study team members to support project execution

Requirements

What you’ll need

Requires at least 2 years independent on-site monitoring experience of interventional studies
Experience across start-up, enrolment, maintenance, close-out
Digital literacy, including confidence using AI tools in a professional setting
Degree in scientific discipline / health care or equivalent industry experience
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Ability to establish and maintain effective working relationships with coworkers and clients
Full UK right to work required
This position is not eligible for visa sponsorship

Benefits

Comp & perks

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
Brandon Hall Excellence Award for Learning & Development