ICON plc
CRC Level 1
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JR159011 CRC Level 1
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.
We are currently seeking a CRC Level 1 to join our team at our Warwickshire clinical research site. This is a fully site-based role and an excellent opportunity for a healthcare professional looking to develop a career in clinical research while continuing to work directly with patients.
As a CRC Level 1, you will play an important role in the day-to-day delivery of clinical trials, supporting participants throughout their study journey and ensuring studies are conducted safely, accurately, and in line with protocol requirements. We are particularly interested in candidates with hands-on clinical experience who are comfortable working directly with patients, performing clinical assessments, and handling study-related documentation and data.
What you will be doing
- 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.
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Your Profile
- Qualification in Nursing, Biomedical Science, Healthcare 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 Us?
This is a fantastic opportunity to join a growing clinical research team and contribute to the development of new medicines and treatments. You'll 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.
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*Please note: This is a fully office/site-based role in Warwickshire. Candidates should be comfortable with regular patient interaction, phlebotomy, clinical procedures, laboratory sample handling, and clinical data entry.
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply.
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