Experienced Clinical Research Associate

Overview

In this role you drive site monitoring across interventional studies, ensuring GCP/ICH compliance and high-quality data. You collaborate with sites to optimize subject recruitment and manage study documentation. You’ll track regulatory submissions, enrollments, CRFs, and data queries while maintaining TMF and ISF accuracy. This position fits within IQVIA’s sponsor-dedicated team and offers growth, flexibility, and a meaningful impact on patient outcomes.

Pay / Benefits

• Flexible working
• Well-being support
• Career development opportunities
• Award and recognition programs
• Professional growth
• Supportive work environment

Responsibilities

• Perform site monitoring visits per scope of work and regulatory standards (GCP/ICH)
• Support site recruitment planning to improve predictability
• Provide protocol training and maintain regular site communication
• Assess site practices for protocol adherence and escalate quality issues
• Track regulatory submissions, recruitment, CRF completion, and data queries
• Assist with start-up activities as needed
• Ensure TMF and ISF documentation is complete and compliant
• Document site management activities and prepare visit reports and follow-up letters
• Collaborate with study team members to support project execution

Key requirements

• Minimum 2 years on-site monitoring experience in interventional studies
• Degree in scientific discipline or health care or equivalent experience
• Strong knowledge of GCP and ICH regulatory requirements
• Ability to build and maintain relationships with coworkers and clients
• UK right to work; visa sponsorship not available

• relationship building
• communication
• collaboration
• GCP
• ICH guidelines
• regulatory submissions

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