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Clinical Research Associate jobs in United Kingdom

Clinical Research Associate - sponsor dedicated

ICON Strategic Solutions

Leeds
On-site
GBP 80,000 - 100,000
Today
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Clinical Specialist/Junior Clinical Research Associate

Thomson Reuters

City of Westminster
On-site
GBP 30,000 - 45,000
2 days ago
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Clinical Research Associate

King's College London

City of Westminster
On-site
GBP 30,000 - 40,000
2 days ago
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Neuroscience Clinical Research Associate (Honorary Doctor)

University of Cambridge

Hartford
On-site
GBP 60,000 - 80,000
Yesterday
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Senior Clinical Research Associate – Oncology Trials

ICON Strategic Solutions

Leeds
On-site
GBP 80,000 - 100,000
Today
Be an early applicant
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Lead Clinical Research Associate

ICON Strategic Solutions

United Kingdom
Remote
GBP 50,000 - 70,000
6 days ago
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Senior Clinical Research Associate (Midwest - Illinois/Michigan)

ICON Strategic Solutions

United Kingdom
Hybrid
GBP 60,000 - 80,000
4 days ago
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Senior Clinical Research Associate

RBW Consulting

Leeds
Remote
GBP 55,000 - 65,000
5 days ago
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Experienced Clinical Research Associate

IQVIA

United Kingdom
On-site
GBP 30,000 - 45,000
3 days ago
Be an early applicant

Clinical Research Associate I: Site Monitoring

AbbVie

Maidenhead
On-site
GBP 30,000 - 45,000
7 days ago
Be an early applicant

Clinical Research Associate I

AbbVie

Maidenhead
On-site
GBP 30,000 - 45,000
7 days ago
Be an early applicant

Clinical Research Associate

ICON Strategic Solutions

United Kingdom
Remote
GBP 40,000 - 60,000
15 days ago

Clinical Research Associate - sponsor dedicated

ICON Strategic Solutions

United Kingdom
On-site
GBP 60,000 - 80,000
12 days ago

Oncology Clinical Research Associate, North-West UK

ICON

England
On-site
GBP 60,000 - 80,000
13 days ago

Clinical Research Associate

King's College London

Greater London
On-site
GBP 45,000 - 68,000
8 days ago

Senior Clinical Research Associate - Oncology, Travel

ICON Strategic Solutions

United Kingdom
On-site
GBP 60,000 - 80,000
12 days ago

Senior Clinical Research Associate - Site Monitoring

IQVIA

Reading
On-site
GBP 30,000 - 50,000
12 days ago

Clinical Research Associate: Psychosis Studies, London

King's College London

Greater London
On-site
GBP 45,000 - 68,000
8 days ago

Clinical Research Associate

BeiGene

United Kingdom
On-site
GBP 40,000 - 60,000
8 days ago

Clinical Research Associate

IQVIA

United Kingdom
On-site
GBP 60,000 - 80,000
15 days ago

UK Clinical Research Associate - Cell & Gene Therapy

ICON Strategic Solutions

United Kingdom
On-site
GBP 60,000 - 80,000
17 days ago

Senior Clinical Research Associate - Scotland

Merck

United Kingdom
Remote
GBP 45,000 - 60,000
22 days ago

Senior Clinical Research Associate (Sr. CRA) - Contractor, UK (CON11HM314)

Aixial Group

Horsham
On-site
GBP 45,000 - 65,000
22 days ago

Oncology Clinical Research Associate, North-West UK

ICON Strategic Solutions

United Kingdom
On-site
GBP 60,000 - 80,000
20 days ago

Oncology Clinical Research Associate — NW UK Trials

ICON Strategic Solutions

United Kingdom
On-site
GBP 60,000 - 80,000
20 days ago

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Clinical Research Associate - sponsor dedicated
ICON Strategic Solutions
Leeds
On-site
GBP 80,000 - 100,000
Full time
Today
Be an early applicant

Job summary

A leading healthcare intelligence firm in the UK is seeking a Senior Clinical Research Associate to oversee clinical trial activities. The role involves monitoring trial sites, ensuring adherence to protocols, and managing relationships with site personnel. Ideal candidates will possess an advanced degree, minimum 12 months of monitoring experience, and oncology experience. The position offers competitive salary and benefits focused on well-being and work-life balance.

Benefits

Various annual leave entitlements
Health insurance offerings
Retirement planning offerings
Employee assistance programme
Flexible optional benefits

Qualifications

  • Minimum of 12 months' monitoring experience required.
  • Strong understanding of clinical trial processes and regulatory requirements.
  • Ability to manage multiple sites and projects simultaneously.

Responsibilities

  • Monitor clinical trial sites for protocol adherence and GCP standards.
  • Conduct site visits to assess performance and resolve issues.
  • Collaborate with teams for data collection and reporting.

Skills

Monitoring experience
Oncology experience
Organizational skills
Communication skills
Stakeholder management skills
Data integrity expertise

Education

Advanced degree in life sciences, nursing, or medicine

Tools

Clinical trial software
Job description
Senior CRA

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 (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile
  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Must have a minimum of 12 months' monitoring experience
  • Must have some Oncology experience
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem‑solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Fluency in English - written and spoken
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should 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.

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, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

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, 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

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.

Are you a current ICON Employee? Please click here to apply

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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