Clinical Research Associate UK - Single Sponsor

ICON Strategic Solutions; Remote; GBP 40,000 - 55,000; Full time

Job summary

A leading clinical research organization in the UK is seeking a Clinical Research Associate to design and analyze clinical trials. The role involves conducting site visits, ensuring compliance with protocols, and contributing to high-quality clinical data. Candidates should have a Bachelor's degree in a relevant field and at least 2 years of experience. This position offers competitive salary and various employee benefits focused on well-being and work-life balance.

Benefits

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of ICH-GCP guidelines.

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits.
• Ensuring protocol compliance and patient safety.
• Collaborating with investigators and site staff.
• Performing data review and query resolution.
• Preparing and reviewing study documentation.

Skills

Clinical trial processes

Organizational skills

Communication skills

Attention to detail

Ability to travel

Education

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

Job description

Clinical Research Associate - UK

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 home‑based Clinical Research Associate II or SCRA to join our diverse and dynamic team.

This is single‑sponsor dedicated – and you’ll be joining an existing team of experienced CRAs already well‑versed in the program requirements.

There is the requirement to attend one remote interview only with the internal Hiring Manager.

As a Clinical Research Associate 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.

Typical 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 resolution of queries to maintain high‑quality clinical data.
• Contributing to the 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 50% of the time and should possess a valid driver’s license.

What ICON can offer you

• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well‑being.
• Life assurance.
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

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.

Visit our careers site to read more about the benefits ICON offers.

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, 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.

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