Clinical study Work, Jobs in Cambridge, Eng (with Salaries)

Clinical Research Associate
TOGL (Holdings) Limited —Cambridge
- Patient monitoring
- In-person
- Communication skills
Quick apply
12d
Band 6 Senior Research Nurse/Senior Clinical Trials Co-ordinator
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £39,959 - £48,117 a year
- Full-time
- University
- Care plans
- Nursing
3d
Clinical Research Nurse - GP Surgery based
St Mary's Surgery —Ely
- Part-time
Quick apply
9d
Medical Affairs Assistant
OGT —Cambridge
- Laboratory experience
- Master's degree
- Bachelor's degree
- Employee discount
Quick apply
Medical Affairs Scientist
OGT —Cambridge
- Laboratory experience
- Bachelor's degree
- Organisational skills
- Employee discount
Quick apply
Scientist I/II, Formulation Development
Abzena Inc. —Cambridge
- £27,000 - £33,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Laboratory experience
Quick apply
10d
Student Health Visitor
Suffolk County Council —Haverhill
- £34,434 a year
- Full-time
- University
- Leadership
- Communication skills
- Annual leave
12d
Laboratory Operations Assistant
TOGL (Holdings) Limited —Cambridge
- Full-time
- Laboratory experience
- English
- Data entry
- Annual leave
Quick apply
9d
Research Governance Administrator
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £25,760 - £27,476 a year
- Full-time
- Microsoft Excel
- Microsoft Office
- Administrative experience
Manager Clinical Operations
MoonLake Immunotherapeutics —Cambridge
- Hybrid work
- Nursing
- Bachelor's degree
- Travel
Quick apply
Bioanalytical Program Lead - UK
LabConnect, LLC —Cambridge
- Full-time
- English
- Bachelor's degree
- Communication skills
Quick apply
Associate Director, Clinical Operations
Jazz Pharmaceuticals —Cambridge
- Remote
- Master's degree
- Bachelor's degree
- No degree
- Annual leave
4d
Clinical Site Manager
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Management
- Machine learning
- Organisational skills
- Annual leave
- Life insurance
Quick apply
Senior Scientist - Molecular Diagnostics (R&D)
TOGL (Holdings) Limited —Cambridge
- Full-time
- Doctoral degree
- Data analysis skills
- Laboratory experience
- Annual leave
Quick apply
5d
Senior Scientist
Cancer Research UK —Babraham
- £41,700 - £51,300 a year
- Full-time
5d
Senior Clinical Site Manager
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Management
- Laboratory experience
- Machine learning
- Annual leave
- Life insurance
Quick apply
Clinical Genomics Consultant
UK Health Security Agency —March
- £94,356 - £150,569 a year
- Part-time
- Hybrid work
- Doctoral degree
- Master's degree
- Presentation skills
3d
Senior QA Auditor - 60% - 80%
Healx —Cambridge
- Part-time
- Hybrid work
- Analysis skills
- Bachelor's degree
- Travel
- Annual leave
- Work from home
Quick apply
Manager, Formulation Development (Analytics)
Abzena Inc. —Cambridge
- £47,000 - £53,000 a year
- Full-time
- Management
- Doctoral degree
- Supervising experience
Quick apply
CYP Manager
Nuffield Health —Cambridge
- £53,600 a year
- Full-time
- Leadership
- Nursing
- Employee discount
- Gym membership
5d

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Clinical Research Associate

TOGL (Holdings) Limited
Cambridge

Quick apply

Job details

12 days ago

Benefits

Company pension

Qualifications

Clinical research
Patient monitoring
Communication skills

Full job description

About The Origin Group Ltd (TOGL)

The Origin Group Limited (TOGL) is the parent organisation and technical service provider to a focused portfolio of UK-based medical technology, research, and innovation companies. Organisations within the group include Origin Sciences, Ellele Health and Biomii. Origin Sciences is a clinical-stage diagnostics company developing and commercialising novel medical devices for gastrointestinal diseases. Our proprietary sample collection technology underpins innovative diagnostic solutions across multiple diagnostic areas with a focus on colorectal cancer.

Ellele Health, is focused on advancing women’s health by developing a novel vaginal sample collection device for gynaecological diagnostics, including the early detection of endometrial cancer.

As a group, we are committed to delivering cutting-edge diagnostic tools that empower clinicians, improve patient outcomes, and transform standards of care.

Role Overview

Reporting to the Head of Clinical Operations, the Study Monitor / Clinical Research Associate is responsible for monitoring clinical studies to ensure they are conducted in accordance with the approved protocol, GCP, applicable regulations, sponsor SOPs and study-specific requirements.

The role provides proactive oversight of study sites, supports high-quality participant protection and data integrity, and ensures that issues are identified, documented, escalated and resolved in a timely and proportionate way. The post-holder will play a critical role in ensuring TOGL clinical studies are delivered safely, efficiently and to a high standard.

Key Responsibilities

Conduct site monitoring activities, including site initiation, interim monitoring and close-out visits, either remotely or on site.
Verify that participants have been consented appropriately and that informed consent documentation is complete, accurate and compliant.
Review source data and eCRF data in line with monitoring plans, with particular focus on critical data, eligibility, safety reporting, sample/device accountability and endpoint data.
Assess site compliance with protocols, GCP, applicable regulations, ethics approvals and sponsor procedures.
Review Investigator Site File documentation and ensure essential documents are complete, current and inspection ready.
Check delegation and training logs to confirm that study activities are performed only by appropriately trained and delegated staff.
Identify, document and follow up protocol deviations, non-compliance, data quality issues and monitoring findings.
Support sites with query resolution, data entry timelines and study process adherence.
Review adverse events, serious adverse events and device deficiencies, where applicable, ensuring reporting is complete and timely.
Maintain clear and accurate monitoring visit reports, follow-up letters and action logs.
Escalate significant or recurring issues to the Clinical Study Manager, Sponsor or relevant study lead.
Support risk-based monitoring activities, including central review of site performance, recruitment, data completeness, query trends and deviation patterns.
Contribute to audit and inspection readiness, including preparation, follow-up and CAPA support.
Build effective working relationships with site teams, investigators, research nurses, data teams and internal study stakeholders.

Requirements

Essential

Minimum 3 years’ experience as a CRA, Study Monitor or equivalent clinical research monitoring role.
Strong working knowledge of ICH-GCP and UK clinical research governance requirements.
Experience conducting remote and/or on-site monitoring visits.
Experience reviewing informed consent, source data, eCRFs, ISF documentation, delegation logs and safety reporting.
Ability to identify and escalate issues affecting participant safety, data integrity or protocol compliance.
Strong written communication skills, including high-quality monitoring reports and follow-up letters.
Excellent attention to detail and ability to manage competing site priorities.
Confident working independently while maintaining clear escalation and oversight.
Good stakeholder management skills and ability to work constructively with NHS site teams.

Desirable

Experience in medical device, IVD, diagnostics or non-CTIMP studies.
Experience with risk-based monitoring approaches.
Familiarity with ISO 14155.

Benefits

25 days holiday
Pension contribution
Competitive salary

Quick apply

Refine Your Search

clinical study jobs in cambridge, eng

Clinical Research Associate

Band 6 Senior Research Nurse/Senior Clinical Trials Co-ordinator

Clinical Research Nurse - GP Surgery based

Medical Affairs Assistant

Medical Affairs Scientist

Scientist I/II, Formulation Development

Student Health Visitor

Laboratory Operations Assistant

Research Governance Administrator

Manager Clinical Operations

Bioanalytical Program Lead - UK

Associate Director, Clinical Operations

Clinical Site Manager

Senior Scientist - Molecular Diagnostics (R&D)

Senior Scientist

Senior Clinical Site Manager

Clinical Genomics Consultant

Senior QA Auditor - 60% - 80%

Manager, Formulation Development (Analytics)

CYP Manager

I want to receive the latest job alerts for clinical study in cambridge, eng

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