Research operations occupations Work, Jobs in Sandy, Bdf (with Salaries)

Clinical Research Associate
TOGL (Holdings) Limited —Cambridge
- Patient monitoring
- In-person
- Communication skills
Quick apply
Associate Director, Clinical Operations
Jazz Pharmaceuticals —Cambridge
- Remote
- Master's degree
- Bachelor's degree
- No degree
- Annual leave
Research Nurse - Oncology
East and North Hertfordshire Teaching NHS Trust —Stevenage
- £39,959 - £48,117 a year
- Full-time
- Flexible schedule
4d
Head of Research and Engagement
Multiple Sclerosis Trust —Letchworth
- £34,032 a year
- Part-time
- Hybrid work
- Analysis skills
- Supervising experience
- Project management
- Free parking
- Annual leave
Quick apply
2d
Trials and Technical Lead
Senova Ltd —Cambridge
- From £35,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Free parking
Quick apply
Research Leader - Monitoring and Evaluation - Defence, Security and Justice
Rand Europe —Cambridge
- From £53,000 a year
- Full-time
- Hybrid work
- Management
- Sales
- English
- Free parking
- Sick pay
Quick apply
Global Clinical Study Lead
Roche —Welwyn
- Bachelor's degree
- No degree
- Leadership
9d
Program Manager
Lonza —Cambridge
- Full-time
- PMP
- Project management
- Business
Clinical Site Manager
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Machine learning
- Organisational skills
- Time management
- Annual leave
- Life insurance
Quick apply
Senior Director, Translational Genetics
GlaxoSmithKline —Stevenage
- £207,075 - £345,125 a year
- Full-time
- Management
- Doctoral degree
- Data analysis skills
- Annual leave
Clinical Advisor -Cell Therapy
AstraZeneca —Cambridge
- Doctoral degree
- Master's degree
- Bachelor's degree
4d
Executive Director, Respiratory
GlaxoSmithKline —Stevenage
- Full-time
- Doctoral degree
- Business development
- Leadership
Biosampling Project Leader
GlaxoSmithKline —Stevenage
- Full-time
- Management
- English
- Bachelor's degree
4d
Geoarchaeology Manager
Cotswold Archaeology —Milton Keynes
- £44,990 - £54,740 a year
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Access
- Annual leave
- Employee assistance programme
Quick apply

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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

research operations occupations jobs in sandy, bdf

Clinical Research Associate

Associate Director, Clinical Operations

Research Nurse - Oncology

Head of Research and Engagement

Trials and Technical Lead

Research Leader - Monitoring and Evaluation - Defence, Security and Justice

Global Clinical Study Lead

Program Manager

Clinical Site Manager

Senior Director, Translational Genetics

Clinical Advisor -Cell Therapy

Executive Director, Respiratory

Biosampling Project Leader

Geoarchaeology Manager

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