Research associate Work, Jobs in Widford, Hrt (with Salaries)

Clinical Research Associate
TOGL (Holdings) Limited —Cambridge
- In-person
- Communication skills
Quick apply
Senior Research Associate - Conjugation
Abcam —Cambridge
- Full-time
- Laboratory experience
- Master's degree
- Bachelor's degree
- Annual leave
2d
Research Associate
Imperial College London —South Kensington
- £43,863 - £57,472 a year
- Full-time
- Research
- Organisational skills
Research Associate
The Brattle Group, Inc. —London
- Research
- Master's degree
- Business development
Research Associate in Translational Neuroimaging
Imperial College London —White City
- £50,733 - £52,675 a year
- Full-time
- Doctoral degree
- Research
- University
Postdoctoral Research Associate - COSPI
City St George's, University of London —London
- Doctoral degree
- Organisational skills
- Training & development
Governance Research Analyst
Broadridge —London
- Full-time
- Databases
- Analysis skills
- Bachelor's degree
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Master's degree
- Business development
- Psychology
- Annual leave
- Gym membership
Associate, Applied Behavioural Research, AI Transformation
Legora —London
- Full-time
- AI
- Communication skills
- Analytics
Operations Associate
Incite —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Writing skills
Quick apply
Market Research Associate (Danish Speaking) - Remote
M3EU —London
- Full-time
- Remote
- Computer literacy
- English
- Analysis skills
Quick apply
Research Technician
Imperial College London —South Kensington
- £42,505 - £47,213 a year
- Full-time
- Doctoral degree
- Laboratory experience
- Research
2d
Research Assistant or Associate in Multifunctional Polymer Composites for Tactile Sensitive Robotic Skin
Imperial College London —South Kensington
- £43,863 - £57,472 a year
- Full-time
- Doctoral degree
- Engineering
- Research
Postdoctoral Research Associate, Criminology
City St George's, University of London —London
- Full-time
- Doctoral degree
- AI
- Communication skills
6d
Associate Director / Associate Principal, Patient-centered Mixed Methods, Survey & Implementation Science Research
IQVIA —London
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Business development
Career Evening at Medpace London - Project Coordinator
Medpace, Inc. —London
- Full-time
- English
- Bachelor's degree
- Organisational skills
- Annual leave
- Work from home
8h
Postdoctoral Research Associate, GUARD project
City St George's, University of London —London
- Full-time
- Doctoral degree
- Computer Science
- Research
Assistant Heritage Consultant
AtkinsRéalis —London
- Full-time
- Hybrid work
- Master's degree
- Project management
NERA Associate Analyst/Analyst - Energy & Natural Resources (London)
Marsh —London
- Full-time
- Hybrid work
- Spanish
- Doctoral degree
- English

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Clinical Research Associate

TOGL (Holdings) Limited
Cambridge

Quick apply

Job details

Benefits

Company pension

Qualifications

Clinical research
Stakeholder collaboration
Stakeholder liaison
Clinical compliance monitoring
Good Clinical Practice (GCP)
Communication skills
Good Clinical Practice (ICH-GCP) guidelines

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

research associate jobs in widford, hrt

Clinical Research Associate

Senior Research Associate - Conjugation

Research Associate

Research Associate

Research Associate in Translational Neuroimaging

Postdoctoral Research Associate - COSPI

Governance Research Analyst

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Associate (Clinical Outcome Assessments - COA)

Associate, Applied Behavioural Research, AI Transformation

Operations Associate

Market Research Associate (Danish Speaking) - Remote

Research Technician

Research Assistant or Associate in Multifunctional Polymer Composites for Tactile Sensitive Robotic Skin

Postdoctoral Research Associate, Criminology

Associate Director / Associate Principal, Patient-centered Mixed Methods, Survey & Implementation Science Research

Career Evening at Medpace London - Project Coordinator

Postdoctoral Research Associate, GUARD project

Assistant Heritage Consultant

NERA Associate Analyst/Analyst - Energy & Natural Resources (London)

I want to receive the latest job alerts for research associate in widford, hrt

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