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5,469

Data Scientist jobs in United Kingdom

Lead Clinical Research Associate

ICON Strategic Solutions

United Kingdom
Remote
GBP 50,000 - 70,000
3 days ago
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Postdoctoral Research Associate in Physical Geography

DURHAM UNIVERSITY

United Kingdom
On-site
GBP 60,000 - 80,000
3 days ago
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Process Scientist/Engineer (FTC)

Femtech Insider Ltd.

North East
On-site
GBP 40,000 - 55,000
3 days ago
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Bacteriology Biomedical Scientist – Band 6 Specialist

Blackpool Teaching Hospitals NHS Foundation Trust

Lancashire
On-site
GBP 30,000 - 40,000
3 days ago
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Pharma Process Scientist/Engineer: Tech Ops & Validation

Femtech Insider Ltd.

North East
On-site
GBP 40,000 - 55,000
3 days ago
Be an early applicant
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Research Associate: Offshore HVDC & Grid Integration

Cardiff University

Cardiff
On-site
GBP 41,000 - 47,000
3 days ago
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Research Associate in Grid integration of renewable power using AC/DC technologies

Cardiff University

Cardiff
On-site
GBP 41,000 - 47,000
3 days ago
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Tenant Researcher, CoStar - London

CoStar Group

City of Westminster
On-site
GBP 25,000 - 35,000
3 days ago
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Biomedical Scientist – Pathology (37.5h, Training)

Dorset County Hospital Nhs Foundation Trust

England
On-site
GBP 60,000 - 80,000
3 days ago
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Specialist Biomedical Scientist

Dorset County Hospital Nhs Foundation Trust

England
On-site
GBP 60,000 - 80,000
3 days ago
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Quantitative Researcher — Securitized Credit Alpha

Man Group

City Of London
On-site
GBP 80,000 - 120,000
3 days ago
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Quantitative Researcher - Securitised

Man Group

City Of London
On-site
GBP 80,000 - 120,000
3 days ago
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TEM Scientist II - Electron Microscopy Specialist

Eurofins Scientific

Lancashire
On-site
GBP 50,000 - 70,000
3 days ago
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TEM Scientist II

Eurofins Scientific

Lancashire
On-site
GBP 50,000 - 70,000
3 days ago
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Research Associate

The University of Manchester

Manchester
Hybrid
GBP 30,000 - 40,000
3 days ago
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Research Associate: Aging Immunity & Breast Cancer

The University of Manchester

Manchester
Hybrid
GBP 30,000 - 40,000
3 days ago
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Lead Freshwater Macroinvertebrate Scientist (Lab)

Apem Ltd

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

Qualitative Paediatric Asthma Research Associate (Hybrid)

University of Leicester

England
Hybrid
GBP 30,000 - 40,000
3 days ago
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Research Associate

University of Leicester

England
Hybrid
GBP 30,000 - 40,000
3 days ago
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Postdoctoral Research Associate

Aston University

Oxford
On-site
GBP 40,000 - 50,000
3 days ago
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Junior LC-MS Bioanalysis Scientist

Oracle

Fordham
On-site
GBP 30,000 - 50,000
3 days ago
Be an early applicant

Scientist I Bioanalysis (LCMS)

Oracle

Fordham
On-site
GBP 30,000 - 50,000
3 days ago
Be an early applicant

NGS Product Development Scientist - Molecular Diagnostics

Taylorollinson

Oxford
On-site
GBP 40,000 - 60,000
3 days ago
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Scientist – Molecular Diagnostics

Taylorollinson

Oxford
On-site
GBP 40,000 - 60,000
3 days ago
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Genomics Lab Scientist — Pathogen Surveillance (Hybrid)

UK Health Security Agency

Idmiston
Hybrid
GBP 30,000 - 40,000
3 days ago
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Lead Clinical Research Associate
ICON Strategic Solutions
Remote
GBP 50,000 - 70,000
Full time
3 days ago
Be an early applicant

Job summary

A leading clinical research organization is seeking a Lead Clinical Research Associate to manage and oversee clinical trial sites, ensuring compliance with study protocols and regulations. The ideal candidate will have extensive experience in the pharmaceutical or biotech industry, with strong leadership and problem-solving skills. Responsibilities include mentoring CRAs and collaborating with cross-functional teams. This role offers a competitive salary and benefits focused on well-being and work-life balance.

Benefits

Annual leave entitlements
Health insurance offerings
Retirement planning
Global Employee Assistance Programme
Life assurance
Flexible optional benefits

Qualifications

  • Extensive experience as a Clinical Research Associate in the pharmaceutical, biotech, or CRO industry.
  • In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
  • Proven track record of managing complex clinical trials.

Responsibilities

  • Leading site management activities for clinical trials.
  • Serving as the primary point of contact for clinical sites.
  • Ensuring integrity of clinical data and protocol compliance.
  • Mentoring and guiding Clinical Research Associates.

Skills

Leadership
Communication
Problem-solving
Organizational skills

Education

Bachelor's degree in life sciences, nursing, pharmacy, or a related field
Advanced degree preferred
Job description
Lead Clinical Research Associate - Ophthalmology

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 Lead Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards. You will be a key contributor to the success of clinical trials by driving site performance, providing mentorship to CRAs, and ensuring the highest levels of data quality and patient safety.

What You Will Be Doing:
  • Leading site management activities, including site selection, initiation, monitoring, and close-out visits, to ensure compliance with study protocols and regulatory guidelines.
  • Serving as the primary point of contact for clinical sites, addressing site queries, and resolving issues to maintain site engagement and performance.
  • Ensuring the integrity of clinical data by conducting thorough source data verification, reviewing site records, and monitoring for protocol deviations.
  • Mentoring and providing guidance to CRAs, contributing to their professional development and supporting the consistent application of best practices across studies.
  • Collaborating with cross-functional teams, including clinical project managers, data managers, and biostatisticians, to ensure the successful execution of clinical trials.
Your Profile:
  • Bachelor's degree in life sciences, nursing, pharmacy, or a related field. Advanced degree preferred.
  • Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO industry, with a proven track record of managing complex clinical trials.
  • In-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
  • Strong leadership and mentoring skills, with the ability to manage and motivate CRAs and site staff effectively.
  • Excellent communication, organizational, and problem-solving skills, with a proactive approach to managing site performance and resolving issues.
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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