At ICON Strategic Solutions, the Clinical Research Associate I works in a sponsor-dedicated model, supported by ICON’s global expertise. The role contributes to clinical trial operations and works collaboratively with the team and stakeholders to deliver high-quality outcomes across clinical programmes. The position involves delivering clinical trial monitoring work to a high standard. The associate coordinates study setup and monitoring activities, maintains study documentation and status reports, handles sponsor-generated queries, supports study cost efficiency, and may participate in preparing and reviewing study documentation and feasibility studies for new proposals. The role also involves working with clinical investigators and site staff to support patient safety and compliance with ICON procedures, study protocols, and regulatory requirements. Travel is approximately 60% as required.
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Job Type
Full-time
Career Level
Entry Level