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Clinical Research Associate

2 months ago


London, Greater London, United Kingdom ICON Full time
Job Title: Clinical Research Associate

At ICON, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the quality and integrity of the data collected.

Key Responsibilities:
  • Evaluate and initiate clinical study sites
  • Monitor and close out clinical study sites
  • Ensure compliance with Good Clinical Practice (GCP) and regulatory requirements
  • Document all activities in clear and comprehensive reports
  • Communicate with investigators, site staff, and sponsor study team members
Requirements:
  • BA/BS in Life Sciences or RN
  • Minimum 2+ years of experience in pharmaceutical/biotechnology industry monitoring
  • Strong Oncology monitoring experience in phase 1-3 clinical trials
  • Good understanding of ICH guidelines, GCP, and regulatory requirements
  • Proficiency in Microsoft Office
  • Ability to handle multiple studies and projects
What We Offer:
  • Competitive salary and benefits package
  • Opportunity to work with a world-leading healthcare intelligence and clinical research organization
  • Chance to develop your skills and expertise in clinical research

At ICON, we value diversity, inclusion, and belonging. We are committed to creating a workplace that is inclusive and respectful of all employees. If you are passionate about clinical research and want to join a dynamic team, please apply for this exciting opportunity.