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ICON plc

Clinical Research Associate

  • UK, Reading · Remote
  • Full-time
  • Posted
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Skills

  • Communication
  • Google Cloud
  • Recruiting

Job description

CRAII - Oncology UK At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

Oncology Clinical Research Associate (All Levels) – UK South-West

Join ICON's FSP Team

ICON's Functional Service Provision (FSP) team is growing, and we're seeking Oncology Clinical Research Associates at all levels to join a dedicated partnership with a long-standing global biopharmaceutical leader.

This is an exciting opportunity to play a key role in advancing innovative oncology research while working within a collaborative, supportive, and highly experienced clinical team. You'll be responsible for overseeing site performance, ensuring data quality and patient safety, and helping to deliver clinical studies that have the potential to improve patients' lives.

What You'll Be Doing

•Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
•Conduct on-site visits across the South West UK region, supporting study sites and identifying solutions to operational challenges.
•Partner with cross-functional teams to ensure accurate, timely collection and reporting of study data.
•Build and maintain strong working relationships with investigators, site staff, and other key stakeholders.
•Provide guidance and support to site personnel, helping to ensure the successful delivery of clinical trials.

What We're Looking For

•A degree in Life Sciences, Nursing, Medicine, or a related discipline.
•Previous UK experience as a Clinical Research Associate within oncology studies.
•Strong understanding of clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP).
•Excellent organisational skills, with the ability to manage multiple sites and priorities effectively.
•Proven experience in site management, monitoring activities, and ensuring high-quality study delivery.
•Strong communication and relationship-building skills.
•Willingness and ability to travel to sites across the UK, with a valid driving licence.

Interested?

If your experience aligns with the above, we'd love to hear from you. Apply today and a member of our recruitment team will be in touch to arrange an informal conversation and discuss the opportunity in more detail.

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