Clinical Research Job at ICON, UK | Life Sciences Candidates, Apply Online
A rare chance has emerged at ICON for aspiring clinical research professionals. The organization is seeking a CRC Level 1 to join its team at the Warwickshire clinical research site. This fully site-based ICON clinical research job offers an excellent opportunity for healthcare professionals to develop a career in clinical research while continuing to engage directly with patients.
- Job Position: CRC Level 1
- Location: Warwickshire, UK
- Job Reference: JR159011
About The Company
ICON is a global healthcare intelligence and clinical research organization dedicated to bringing new medicines and treatments to patients faster. With a mission centered around integrity, collaboration, agility, and inclusion, ICON emphasizes the importance of these values in all interactions with customers, patients, and suppliers.
ICON Clinical Research Job Description
The CRC Level 1 will play a crucial role in the day-to-day delivery of clinical trials, supporting participants throughout their study journey. This ICON clinical research job requires hands-on clinical experience, with responsibilities that include conducting clinical assessments and managing study-related documentation and data.
Clinical Research Job – Key Responsibilities
- Supporting the delivery and coordination of clinical trial activities.
- Recruiting, screening, and enrolling study participants.
- Conducting participant visits and supporting patients throughout the clinical trial process.
- Performing protocol-required clinical procedures, including:
- Phlebotomy and sample processing
- Vital signs assessments
- ECGs and other study-specific procedures
- Collection and documentation of clinical data
- Maintaining accurate source documentation and study records.
- Entering study data into Electronic Data Capture (EDC) systems and resolving data queries.
- Supporting study start-up activities, participant recruitment, and retention efforts.
- Maintaining regulatory documentation and ensuring compliance with study protocols and SOPs.
- Working closely with Investigators, sponsors, and monitors to support successful study delivery.
- Supporting monitoring visits, audits, and inspection readiness activities.
- Educating participants about study requirements and the clinical trial process.
- Assisting with participant reimbursement and study administration activities.
Eligibility Criteria Required For Clinical Research Job
- Qualification in Biomedical Science, Life Sciences, or another relevant healthcare discipline.
- Previous healthcare experience involving direct patient contact is highly desirable.
- Experience with phlebotomy, sample handling, clinical observations, or other patient-facing clinical procedures would be advantageous.
- Strong attention to detail and excellent documentation skills.
- Comfortable working with both patients and clinical data.
- Good organizational skills and the ability to manage multiple tasks effectively.
- Strong communication and interpersonal skills.
- Proficiency in Microsoft Office applications and confidence working with electronic systems.
- An interest in clinical research and developing a career within the clinical trials industry.
Why Join ICON?
This is a fantastic opportunity to join a growing clinical research team and contribute to the development of new medicines and treatments. Candidates will gain hands-on experience across a variety of clinical studies while working in a supportive environment where patient care and research excellence go hand in hand.
The opportunity at ICON for the CRC Level 1 role presents an excellent pathway for healthcare professionals to advance their careers through this ICON clinical research job. Interested candidates are encouraged to apply before the deadline to seize this opportunity.
