Clinical study Work, Jobs in Sandy, Bdf (with Salaries)

Clinical Research Associate
TOGL (Holdings) Limited —Cambridge
- Patient monitoring
- In-person
- Communication skills
Quick apply
13d
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
4d
Study Manager - 1 year FTC
Roche —Welwyn
- Hybrid work
- Bachelor's degree
Laboratory Operations Assistant
TOGL (Holdings) Limited —Cambridge
- Full-time
- Laboratory experience
- English
- Data entry
- Annual leave
Quick apply
10d
Scientist I/II, Formulation Development
Abzena Inc. —Cambridge
- £27,000 - £33,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Laboratory experience
Quick apply
11d
Medical Affairs Scientist
OGT —Cambridge
- Laboratory experience
- Bachelor's degree
- Organisational skills
- Employee discount
Quick apply
Trainee Solicitor
Medical Defence Shield —Bromham
- £30,000 - £35,000 a year
- Full-time
- Hybrid work
- English
- Microsoft Office
- Administrative experience
- Work from home
Quick apply
3d
Senior Scientist - Molecular Diagnostics (R&D)
TOGL (Holdings) Limited —Cambridge
- Full-time
- Doctoral degree
- Data analysis skills
- Laboratory experience
- Annual leave
Quick apply
6d
Graduate Research Scientist- Bioanalysis LC-MS
Pharmaron —Rushden
- Laboratory experience
- Microsoft Office
- Bachelor's degree
Quick apply
Medical Affairs Assistant
OGT —Cambridge
- Laboratory experience
- Master's degree
- Bachelor's degree
- Employee discount
Quick apply
Ambulance Care Assistant - Student Paramedics
Rapid Response Ambulance (RRA) —Wellingborough
- £12.80 - £14.00 an hour
- First Aid Certification
- Patient care
- In-person
- Employee discount
Quick apply
6d
Advanced Pain Clinician
Cora Health —Milton Keynes
- £44,805 - £61,156 a year
- Full-time
- Hybrid work
- Management
- Employee assistance programme
6d
Bioanalytical Program Lead - UK
LabConnect, LLC —Cambridge
- Full-time
- English
- Bachelor's degree
- Communication skills
Quick apply
Country Study Start-Up Team Leader (cSTL)
Roche —Welwyn
- Management
- Doctoral degree
- English
Laboratory Support - DMPK
Charles River Laboratories —Saffron Walden
- Full-time
- Sales
- Laboratory experience
- Paid training
- Annual leave
1d
Research Governance Administrator
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £25,760 - £27,476 a year
- Full-time
- Microsoft Excel
- Microsoft Office
- Administrative experience
Senior Scientist
Cancer Research UK —Babraham
- £41,700 - £51,300 a year
- Full-time
6d
Associate Director, Clinical Operations
Jazz Pharmaceuticals —Cambridge
- Remote
- Master's degree
- Bachelor's degree
- No degree
- Annual leave
5d
General Practitioner
Bupa —Milton Keynes
- Part-time
- BLS Certification
- Microsoft Office
- IT
- Employee discount
- Gym membership
Quick apply
Manager Clinical Operations
MoonLake Immunotherapeutics —Cambridge
- Hybrid work
- Nursing
- Bachelor's degree
- Travel
Quick apply

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clinical study jobs near sandy, bdf

Clinical Research Associate

TOGL (Holdings) Limited
Cambridge

Quick apply

Job details

13 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 sandy, bdf

Clinical Research Associate

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

Study Manager - 1 year FTC

Laboratory Operations Assistant

Scientist I/II, Formulation Development

Medical Affairs Scientist

Trainee Solicitor

Senior Scientist - Molecular Diagnostics (R&D)

Graduate Research Scientist- Bioanalysis LC-MS

Medical Affairs Assistant

Ambulance Care Assistant - Student Paramedics

Advanced Pain Clinician

Bioanalytical Program Lead - UK

Country Study Start-Up Team Leader (cSTL)

Laboratory Support - DMPK

Research Governance Administrator

Senior Scientist

Associate Director, Clinical Operations

General Practitioner

Manager Clinical Operations

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