CRA II

ICON Strategic Solutions; United Kingdom; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in the United Kingdom is seeking a Clinical Research Associate II to ensure quality in clinical trials. You'll conduct site visits, ensure compliance, and analyze clinical data. Applicants need a Bachelor's degree and a minimum of 2 years’ experience. This role offers a competitive salary along with various health and wellness benefits to support work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Responsibilities

• Conduct site qualification, initiation, monitoring and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolution of queries to maintain high-quality clinical data.
• Contribute to preparation and review of study documentation.

Skills

Organizational skills

Communication skills

Attention to detail

Ability to work independently

Ability to travel

Education

Bachelor’s degree in a scientific or healthcare-related field

Job description

Clinical Research Associate - Oncology - UK Studies

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• Conduct site qualification, initiation, monitoring and close‑out visits for clinical trials.
• Ensure protocol compliance, data integrity and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolution of queries to maintain high‑quality clinical data.
• Contribute to preparation and review of study documentation, including protocols and clinical study reports.

Your profile

• Bachelor’s degree in a scientific or healthcare‑related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• 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.
• Ability to travel at least 60% of the time (international and domestic) and possess a valid driver’s license.

What ICON can offer you

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.

• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings.
• Global Employee Assistance Programme, LifeWorks.
• Life assurance.
• Flexible country‑specific optional benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, and more.

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, colour religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If you need a reasonable accommodation for any part of the application process, please let us know or submit a request.

Interested in the role, but unsure if you meet all of the requirements? We encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for at ICON, whether for this role or other roles.