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# CRC Level 1

- **Company:** ICON plc
- **Location:** London, UK
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Software Applications, Microsoft Outlook, Databases, Electronic Data Capture, Microsoft Office
- **Published:** August 6, 2026
- **Apply:** https://dejobs.org/x/x/99713DC6C98B45AB8B8070B7209ADD97/job/

## About the Role

* Bachelor's degree in life sciences, healthcare, or related field; relevant experience may be considered in lieu of a degree.
 * Previous experience in clinical research or healthcare setting is preferred but Nt required.
 * Strong organizational skills and attention to detail, with the ability to manage multiple tasks and priorities effectively.
 * Excellent communication and interpersonal skills, with the ability to interact professionally with study participants and colleagues.
 * Proficiency in Microsoft Office suite (Word, Excel, Outlook) and willingness to learn new software applications as needed.

## Description

* Assisting in the coordination and implementation of clinical trial activities under the guidance of Clinical Research Coordinators (CRCs), including patient recruitment, screening, and enrollment.
 * Supporting the maintenance and organization of study documentation and regulatory files, ensuring compliance with protocol requirements and regulatory standards.
 * Collecting, recording, and entering data into study databases and electronic data capture (EDC) systems, in accordance with study protocols and standard operating procedures (SOPs).
 * Assisting with the preparation and submission of regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs).
 * Providing logistical support for study visits, meetings, and other research-related activities, including scheduling appointments, arranging travel, and coordinating study materials.