Clinical data manager Work, Jobs in Saffron Walden, Ess (with Salaries)

Clinical Research Associate
TOGL (Holdings) Limited —Cambridge
- Patient monitoring
- In-person
- Communication skills
Quick apply
Experienced Phlebotomist for Chelmsford
Sussex Pathology Limited (onedaytests.com) —Chelmsford
- £18 an hour
- Part-time
- Inventory control
- Customer service
- Travel
- Annual leave
Quick apply
Data Processor
PCN North —Stevenage
- Part-time
- Medication administration
- Microsoft Office
- Administrative experience
- Free parking
- Store discount
Quick apply
2d
PCN Manager and Digital & Transformation Lead
PrimaryCareCareers —Letchworth
- Continuous improvement
- No degree
- Organisational skills
6d
Global Medical Advisor - Rescue Treatments
Mundipharma —Cambridge
- Full-time
- Doctoral degree
- Communication skills
Clinical Team Administrator
NHS Professionals —Bury St. Edmunds
- £14.05 an hour
- Temporary
- Management
- Customer service
- Word processing
Quick apply
1d
Data Partnerships Project Manager
Qureight Ltd —Cambridge
- £56,000 - £61,000 a year
- Full-time
- Hybrid work
- Annual leave
- Life insurance
Quick apply
14d
Data Operations Officer
Alzheimer's Research UK —Cambridge
- £32,000 a year
- CRM software
- Microsoft Excel
- Salesforce
- Sick pay
Rostering Manager
The Princess Alexandra Hospital NHS Trust —Harlow
- £49,387 - £56,515 a year
- Management
- Continuous improvement
19h
Senior Scientist - Molecular Diagnostics (R&D)
TOGL (Holdings) Limited —Cambridge
- Full-time
- Doctoral degree
- Data analysis skills
- Laboratory experience
- Annual leave
Quick apply
Children and Young Peoples' Independent Sexual Violence Advocate (ChISVA)
Cambridge Rape Crisis Centre —Cambridge
- £28,505 a year
- Full-time
- Travel
- Computer skills
- In-person
- Free parking
- Annual leave
Quick apply
Quality Development Manager FTC
Care UK —Writtle
- Nursing
9d
Scientist I/II, Formulation Development
Abzena Inc. —Cambridge
- £27,000 - £33,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Laboratory experience
Quick apply
Delivery Director of Workforce Planning and Resourcing
HUC —Welwyn Garden City
- £95,000 a year
- Full-time
Better at Home Call Handler
Watford & Three Rivers Trust —Hertford
- £23,660 a year
- Weekend availability
- Remote
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
Head of Quality Assurance and Regulatory Affairs
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Project management
- Bachelor's degree
- Continuous improvement
- Annual leave
- Life insurance
Quick apply
13d
Senior Scientist - Assay Verification Molecular Diagnostics
TOGL (Holdings) Limited —Cambridge
- Full-time
- Doctoral degree
- Master's degree
- Annual leave
Quick apply
Transfusion Practitioner
The Princess Alexandra Hospital NHS Trust —Harlow
- £39,959 - £48,117 a year
- Hospice
19h
Project Manager (AI models)
Qureight Ltd —Cambridge
- £56,000 - £61,000 a year
- Full-time
- Hybrid work
- Machine learning
- AI
- Communication skills
- Annual leave
- Life insurance
Quick apply
14d
Legacy and In-Memory Manager
Essex & Herts Air Ambulance —Marks Tey
- £40,000 - £45,000 a year
- Full-time
- Organisational skills
- Annual leave
- Employee assistance programme

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clinical data manager jobs near saffron walden, ess

Clinical Research Associate

TOGL (Holdings) Limited
Cambridge

Quick apply

Job details

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 data manager jobs in saffron walden, ess

Clinical Research Associate

Experienced Phlebotomist for Chelmsford

Data Processor

PCN Manager and Digital & Transformation Lead

Global Medical Advisor - Rescue Treatments

Clinical Team Administrator

Data Partnerships Project Manager

Data Operations Officer

Rostering Manager

Senior Scientist - Molecular Diagnostics (R&D)

Children and Young Peoples' Independent Sexual Violence Advocate (ChISVA)

Quality Development Manager FTC

Scientist I/II, Formulation Development

Delivery Director of Workforce Planning and Resourcing

Better at Home Call Handler

Head of Quality Assurance and Regulatory Affairs

Senior Scientist - Assay Verification Molecular Diagnostics

Transfusion Practitioner

Project Manager (AI models)

Legacy and In-Memory Manager

I want to receive the latest job alerts for clinical data manager in saffron walden, ess

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