Clinical Research Associate monitoring
Listed on 2026-06-11
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Medical Science
Icon plc is a world‑leading healthcare intelligence and clinical research organization. You’re invited to join us on our mission to shape the future of clinical development.
Job titleCRA (must have at least 12 months’ monitoring experience)
LocationMust be based in the UK
Fully sponsor dedicated
Role OverviewWorking fully embedded within a growing program as a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will DoYou will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities- Conducting site qualification, initiation, monitoring, and close‑out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolving queries to maintain high‑quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required Qualifications And Experience- Bachelor’s degree in a scientific or healthcare‑related field.
- Minimum of 12 months experience as a Clinical Research Associate.
- Must have experience working on Oncology trials.
- In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast‑paced environment.
- Willingness to travel as required (approximately 60 %)
In addition to your competitive salary, ICON offers a range of additional benefits focused on well‑being and work‑life balance.
Our Benefits Examples Include- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, Life Works, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who support you and your family’s well‑being.
- Life assurance
- Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
#J-18808-LjbffrTo Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search: