Clinical Trial Associate – London (On-site 2 days)

Overview

ICON is seeking a Clinical Trial Associate in London to assist in designing and analyzing clinical trials. The role involves coordinating trials, maintaining documentation, preparing study materials, and ensuring compliance with regulatory standards.

Responsibilities

• Assist in designing and analyzing clinical trials
• Coordinate clinical trials
• Maintain documentation
• Prepare study materials
• Ensure compliance with regulatory standards

Qualifications

• Bachelor’s degree in a scientific field
• Relevant clinical research experience
• Strong organizational skills

Benefits

• Health insurance
• Retirement planning
• Annual leave entitlements

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