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3,271

Research Scientist jobs in United Kingdom

Sr. Clinical Research Associate (United Kingdom)

Allucent

London
Hybrid
GBP 60,000 - 80,000
13 days ago
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Equity Research Associate

Jefferies

London
On-site
GBP 80,000 - 100,000
13 days ago

Equity Research, Associate (London)

RBC

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

Associate Research Practitioner | Frimley Health NHS Foundation Trust

Frimley Health NHS Foundation Trust

Camberley
On-site
GBP 24,000 - 30,000
13 days ago

Clinical Research Associate

Kings College London

London
On-site
GBP 30,000 - 40,000
14 days ago
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Sustainable Investing Research Analyst , VP - State Street Investment Management - State Street C...

ZipRecruiter

London
On-site
GBP 125,000 - 150,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Norwich
Hybrid
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Swindon
Hybrid
GBP 60,000 - 80,000
30+ days ago
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Capital Research Analyst (Premium wine)

JR United Kingdom

Milton Keynes
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Stevenage
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Telford
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Dartford
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

York
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Stoke-on-Trent
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Warrington
Remote
GBP 30,000 - 50,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Glasgow
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

North East
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Oxford
Hybrid
GBP 80,000 - 100,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Colchester
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Stockport
Hybrid
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Cardiff
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Chelmsford
Hybrid
GBP 25,000 - 35,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

London
Remote
GBP 30,000 - 50,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Liverpool
Remote
GBP 60,000 - 80,000
30+ days ago

Capital Research Analyst (Premium wine)

JR United Kingdom

Doncaster
Remote
GBP 60,000 - 80,000
30+ days ago

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Sr. Clinical Research Associate (United Kingdom)
Allucent
London
Hybrid
GBP 60,000 - 80,000
Full time
13 days ago

Job summary

A biopharmaceutical firm in London is seeking a Sr. Clinical Research Associate to lead monitoring activities for clinical trials. You will ensure compliance, build strong relationships with sites, and manage trial integrity. The ideal candidate has over 5 years of experience and knowledge of regulatory guidelines. This role offers a competitive salary and opportunities for professional development, and requires travel within the UK.

Benefits

Competitive salaries and comprehensive benefits package
Departmental Study/Training for professional development
Mentoring opportunities
Internal growth opportunities
Employee referral program
Employee recognition programs
Loyalty Award Program

Qualifications

  • Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of 5 years’ experience.
  • Strong understanding of ICH-GCP and regulatory guidelines.
  • Clear and confident communicator in English.
  • Comfortable working independently and managing priorities.
  • Willingness to travel, as required.

Responsibilities

  • Independently manage all aspects of monitoring for assigned clinical trials.
  • Ensure compliance with protocols, GCP, ICH, SOPs.
  • Build strong site relationships, acting as primary point of contact.
  • Identify and resolve site issues to maintain trial integrity.
  • Activities around regulatory affairs, site activation and study-startup.

Skills

Clinical trial management
Regulatory compliance
Communication
Problem-solving
Job description
Overview

Bring your monitoring expertise to the forefront of innovation. We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid). As a Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. At Allucent we are big enough to deliver and small enough to care. We know all our colleagues by name and work together as a team to make everyone SHINE.

The role

As a Sr. CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. This includes work related to regulatory affairs, site activation processes—including contracting and start-up activities—to ensure smooth and compliant study execution. You will travel throughout The UK.

Main responsibilities
  • Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
  • Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
  • Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
  • Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
  • Activities around regulatory affairs, site activation and study-startup.
Qualifications
  • Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 5 years’ experience.
  • Strong understanding of ICH-GCP and regulatory guidelines.
  • Clear and confident communicator in English.
  • Comfortable working independently and managing priorities.
  • Willingness to travel, as required.
Benefits
  • Competitive salaries and a comprehensive benefits package
  • Departmental Study/Training for furthering professional development
  • Mentoring opportunities
  • Internal growth opportunities and career progression
  • Financially rewarding internal employee referral program
  • Eligibility for our internal employee recognition programs for going above and beyond on projects
  • Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees
About Allucent

At Allucent, our mission is to shine a light on new therapies that improve lives. When you join our team, you’ll use your unique skills, expertise, and knowledge to forge meaningful partnerships with clients while helping them turn groundbreaking ideas into life-changing treatments.

If you’re passionate about advancing pharmaceuticals and biologics, fueled by an entrepreneurial spirit, and eager to collaborate with top minds across science, business, and operations, we’d love to connect. Together we can accelerate innovation and grow side by side, making a last impact on patients worldwide.

Together we SHINE. Find more information about our values.

Apply

Apply now! If you are interested in this role please apply through the button or for more information reach out to Yael Kokernoot, yael.kokernoot@allucent.com

Disclaimers

*Our in-office work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

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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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