Patient safety manager Work, Jobs in Babraham, Cam (with Salaries)

Clinical Research Associate
TOGL (Holdings) Limited —Cambridge
- In-person
- Communication skills
Quick apply
Senior Facilities Co-Ordinator
Lifeplus Europe Ltd —St. Neots
- £35,000 - £40,000 a year
- Hybrid work
- Travel
- Employee assistance programme
- Employee discount
Quick apply
Point of Care Service Manager
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £49,387 - £56,515 a year
- Part-time
- Management
- Master's degree
- Databases
1d
Trainee Education Mental Health Practitioner (EMHP)
East of England Community Health and Care NHS Trust (Cambridgeshire) —Cambridge
- £28,392 - £31,157 a year
- Full-time
- Research
- University
- Experience working with children
6d
Senior Facilities Manager, UK & I
JAA-Jones Lang LaSalle Limited —Cambridge
- Full-time
- Bachelor's degree
- Team management
- Recruiting
Quick apply
Global Patient Safety Business Excellence, Senior Manager
Amgen —Cambridge
- PMP
- Continuous improvement
- Agile
6d
Clinical Governance Manager
The Day Clinic —Cambridge
- From £20 an hour
- Part-time
- Microsoft Excel
- Data analysis skills
- English
- Free parking
- Flexitime
Quick apply
10d
Senior Scientific Associate [Temporary Cover]
University of Cambridge —Cambridge
- £35,608 - £46,049 a year
- Full-time
- Laboratory experience
9d
Quality Assurance Team Leader
Medirest —Cambridge
- £31,089.20 a year
- Data analysis skills
- Analysis skills
- Continuous improvement
18h
Associate Director, Head of High Throughput Lab
Flagship Pioneering, Inc. —Cambridge
- Doctoral degree
- Master's degree
- Continuous improvement
4d
R&D Quality Manager
Sandoz —Cambridge
- Full-time
- English
- Project management
- Quality control
- Annual leave
Lab Operations Manager
Avantor —Cambridge
- Full-time
- Continuous improvement
- AI
- Leadership
Patient Services Co-ordinator
PrimaryCareCareers —Clare
- Microsoft Office
- Communication skills
3d
PALS Officer
West Suffolk NHS Foundation Trust —Bury St. Edmunds
- £28,392 - £31,157 a year
- Part-time
- Databases
- Communication skills
1d
Research Assistant (Fixed Term)
University of Cambridge —Cambridge
- £33,002 - £35,608 a year
- Research
- University
6d
CQC Registered Manager
Live In Carer —Cambridge
- From £40,000 a year
- Temporary
- Medication administration
- Experience working with individuals with disabilities
- Nursing home
Quick apply
Patient Services Coordinator
Guildhall Surgery —Clare
- £12.87 an hour
- Part-time
- In-person
Quick apply
6d
Research Pipeline Project Manager
GlaxoSmithKline —Stevenage
- Full-time
- Hybrid work
- Doctoral degree
- PMP
- Engineering
Trainee Dispenser
Boots —Cambridge
- £16 an hour
- Weekend availability
- No experience needed
- Employee assistance programme
- Employee discount
Trainee Bus Driver (including Apprenticeship qualification)
Stagecoach —Cambridge
- £35,424 a year
- Weekend availability
- Customer service
- No experience needed
- School
- Paid training
- Employee assistance programme

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patient safety manager jobs near babraham, cam

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

patient safety manager jobs in babraham, cam

Clinical Research Associate

Senior Facilities Co-Ordinator

Point of Care Service Manager

Trainee Education Mental Health Practitioner (EMHP)

Senior Facilities Manager, UK & I

Global Patient Safety Business Excellence, Senior Manager

Clinical Governance Manager

Senior Scientific Associate [Temporary Cover]

Quality Assurance Team Leader

Associate Director, Head of High Throughput Lab

R&D Quality Manager

Lab Operations Manager

Patient Services Co-ordinator

PALS Officer

Research Assistant (Fixed Term)

CQC Registered Manager

Patient Services Coordinator

Research Pipeline Project Manager

Trainee Dispenser

Trainee Bus Driver (including Apprenticeship qualification)

I want to receive the latest job alerts for patient safety manager in babraham, cam

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