Clinical Research Associate

Responsibilities

• Site qualification, initiation, monitoring, and close-out visits
• Building strong relationships with investigators and site staff
• Driving data quality, protocol compliance, and study execution
• Supporting patient recruitment and site performance
• Maintaining inspection-ready study documentation
• Collaborating cross-functionally with Clinical Operations and study teams

Benefits

• Competitive salary and benefits
• Exposure to both clinical and commercial aspects of drug development
• Direct interaction with world-class scientific experts
• Significant career growth potential within a fast-growing organization
• EPM Scientific is proud to be a leading specialist recruitment agency for the life sciences industry.
• London, England, GBR
• https://www.epmscientific.com/
• Late Stage
• Leadership Team
• Sean P.
• Senior Vice President Commercial - Field at EPM Scientific
• Recent News
• BioSpace
• CDMO hiring tough as demand for specialized talent outpaces supply
• 2026-08-26
• BioSpectrum Asia
• What's Transforming Australia's Thriving Life Sciences Industry?
• 2023-12-23
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• AI Tools
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• Analyze How Well You Fit
• Understand your strength & weakness

Qualifications

• 2-4 years of clinical research experience
• CRA, Clinical Research Coordinator, or similar clinical operations background
• Independent monitoring experience
• Strong understanding of ICH-GCP and clinical trial conduct
• Passion for quality, collaboration, and improving patient outcomes

Required skills

• Clinical Research, Clinical Trial Conduct, Clinical Trial Monitoring, ICH-GCP

Experience

• 2-4 years