Clinical Research jobs in United Kingdom
Explore 37 matching jobs.
Clinical Research Associate
ICON plc
Posted: 10/20/2026Clinical Research Associate – Level 1
ICON plc
Posted: 10/15/2026Clinical Study Manager
ICON plc
Posted: 10/14/2026Senior Clinical Data Manager
Qureight
Posted: 10/13/2026Senior Clinical Data Manager – Data Standards
ICON plc
Posted: 10/12/2026Principal Biostatistician, Senior Biostatistician – R/Rshiny
Syneos Health
Posted: 10/12/2026Business Development Director – Clinical Research
ERGOMED
Posted: 10/9/2026Clinical Trial Manager I/II
ICON plc
Posted: 10/8/2026Clinical Data Manager
Worldwide Clinical Trials
Posted: 10/7/2026Clinical Trial Manager – Regulatory Submissions
ICON plc
Posted: 10/7/2026Senior Biostatistician – Biomarker Experience
ICON plc
Posted: 10/6/2026Biostatistician – Biomarker Experience
ICON plc
Posted: 10/6/2026Senior Clinical Research Associate II – UK
CTI Clinical Trial and Consulting Services
Posted: 10/2/2026Biostatistician
Celerion
Posted: 9/30/2026Head of Clinical Research
Endure Capital
Posted: 9/30/2026Principal Biostatistician – FSP
Clinical Outcomes Solutions
Posted: 9/29/2026Clinical Research Associate
IQVIA
Posted: 9/29/2026Senior Clinical Data Manager
Precision For Medicine
Posted: 9/29/2026Senior Clinical Data Manager
Precision Medicine Group
Posted: 9/29/2026Senior Clinical Research Associate – Oncology
Parexel
Posted: 9/24/2026Core Competencies
Role fitUse this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trial activities, ensuring adherence to protocols and regulatory requirements while fostering collaboration across teams. Proficient in monitoring practices and site management, with strong organizational and communication skills to drive compliance and support trial execution.
About the role
Key responsibilities & impact- Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
- Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
- Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
- Conduct site visits to assess performance, resolve issues, and support successful trial execution
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs
- Build and maintain relationships with site personnel and stakeholders to facilitate smooth trial operations
Requirements
What you’ll need- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- 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 (fluency in English), interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
- Willingness to travel as required (domestic travel)
- Driving licence
- Legal right to work in the country where the role is based
Benefits
Comp & perks- 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
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