Clinical research associate Work, Jobs in Southfields, Gtl (with Salaries)

Clinical Research Associate, South East England
IQVIA —London
- Full-time
- Maintenance
- No degree
6d
Research Associate in Salmonella clinical study
Imperial College London —South Kensington
- £43,863 - £57,472 a year
- Full-time
- Hybrid work
- Doctoral degree
- University
- Organisational skills
Research Associate
Lumanity —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Research Associate
Imperial College London —Hammersmith
- £49,017 - £57,472 a year
- Full-time
- Doctoral degree
- University
Research Associate in Cancer Microbiology
Imperial College London —Hammersmith
- £49,017 - £52,922 a year
- Full-time
- Doctoral degree
- Communication skills
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Clinical Quality Assurance - Program Lead (Associate Director)
Novartis —London
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Research Associate* in Trustworthy MRI Reconstruction with Uncertainty Modelling
Imperial College London —South Kensington
- £43,863 - £57,472 a year
- Full-time
- Doctoral degree
- Master's degree
- Analysis skills
8d
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Project management
Quick apply
Research Associate in Artificial Intelligence & Machine Learning
Imperial College London —Hammersmith
- £43,863 - £55,144 a year
- Full-time
- Doctoral degree
- University
- Machine learning
9d
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Research Associate in Surgical Vision and AI
Imperial College London —South Kensington
- £49,017 - £52,922 a year
- Full-time
- Doctoral degree
- C++
- Machine learning
CRA II / Sr CRA I - Multi-Sponsor
サイネオス・ヘルス —London
- Bachelor's degree
- Travel
- Contracts
Manager - Patient Experience Data
IQVIA —London
- Full-time
- Remote
- Project management
- IT
- Time management
2d
Research Fellow in Brain Vascular Biology and Brain Cancer Biology
University College London —London
- £43,374 - £51,860 a year
- Full-time
- Doctoral degree
- English
- University
- Annual leave
- Employee assistance programme
Postdoctoral Research Associate, DASH
City St George's, University of London —London
- Full-time
- Doctoral degree
- Analysis skills
- University
Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
- Communication skills
Senior Translation Executive
Cancer Research UK —Stratford
- £68,000 - £72,000 a year
- Full-time
- Doctoral degree
- Travel
- Mentoring
5d
Global Program Clinical Head (Neuroscience)
Novartis —London
- Full-time
- Hybrid work
- Doctoral degree
- Communication skills
Trial Vendor Associate Director
Novartis —London
- Full-time
- Hybrid work
- Communication skills
13d

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clinical research associate jobs near southfields, gtl

Clinical Research Associate, South East England

IQVIA -
London

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Job details

Full-time
6 days ago

Qualifications

Clinical research
Maintenance

Full job description

London, United Kingdom | Full time | Field-based | R1550636

Join IQVIA on our mission to accelerate innovation for a healthier world!

IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England.

Why IQVIA?

Career development opportunities to grow as we grow
AI‑powered career advancement through our internal talent marketplace, Career Connections
Mentorship opportunities across the organisation via Employee Resource Groups
Flexible working to assist work–life balance and professional success
Well‑being support covering your physical, mental, and financial health

Awards

2026 "Glassdoor Best Place to Work in the UK"
#1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)
Brandon Hall Excellence Award for Learning & Development

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Collaborate and liaise with study team members for project execution support as appropriate

Requirements

Requires at least 6 months independent on-site monitoring experience of interventional studies
Experience across start-up, enrolment, maintenance, close-out
Digital literacy, including confidence using AI tools in a professional setting
Degree in scientific discipline / health care or equivalent industry experience
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Ability to establish and maintain effective working relationships with coworkers and clients
Full UK right to work required, this position is not eligible for visa sponsorship

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

#LI-ADAMTHOMPSON

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

Refine Your Search

clinical research associate jobs in southfields, gtl

Clinical Research Associate, South East England

Research Associate in Salmonella clinical study

Research Associate

Research Associate

Research Associate in Cancer Microbiology

Clinical Trial Associate Manager

Clinical Quality Assurance - Program Lead (Associate Director)

Research Associate* in Trustworthy MRI Reconstruction with Uncertainty Modelling

Study Manager, Clinical Operations

Research Associate in Artificial Intelligence & Machine Learning

Clinical Trials Manager

Research Associate in Surgical Vision and AI

CRA II / Sr CRA I - Multi-Sponsor

Manager - Patient Experience Data

Research Fellow in Brain Vascular Biology and Brain Cancer Biology

Postdoctoral Research Associate, DASH

Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)

Senior Translation Executive

Global Program Clinical Head (Neuroscience)

Trial Vendor Associate Director

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