Research associate Work, Jobs in Tormarton, Gls (with Salaries)

Clinical Research Associate, South West England
IQVIA —Bath
- Full-time
- Maintenance
- No degree
Research Associate
University of Bath —Bath
- £38,784 - £46,049 a year
- Full-time
- Doctoral degree
- Engineering
- Data analysis skills
- Annual leave
- Employee discount
12d
Clinical Research Associate II, South West England
IQVIA —Bath
- Full-time
- Maintenance
- No degree
Research Associate in Atmospheric Dynamics for High-Altitude Autonomous Platforms
University of Bath —Bath
- £38,784 - £46,049 a year
- Full-time
- Doctoral degree
- Maths
- University
- Annual leave
- Employee discount
9d
Research Associate in Atmospheric Dynamics
University of Bath —Bath
- £38,784 - £46,049 a year
- Full-time
- Doctoral degree
- Maths
- University
- Annual leave
- Employee discount
4d
Research Associate in Quantum Fibre Photonics
University of Bath —Bath
- £38,784 - £46,049 a year
- Full-time
- Doctoral degree
- University
- Annual leave
- Employee discount
13d
Research Technician
University of Bristol —Bristol
- £28,778 - £32,080 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Laboratory experience
10d
Responsible AI/ML Scientist (KTP Associate)
University of Bristol —Bristol
- £50,000 - £60,000 a year
- Full-time
- Doctoral degree
- Computer Science
- Master's degree
3d
Senior Research Associate in Petrological Controls on Ore Genesis
University of Bristol —Bristol
- £43,482 - £50,253 a year
- Full-time
- Doctoral degree
- University
- Travel
11d
Research Associate in QET LABS /Senior Research Associate
University of Bristol —Bristol
- £37,099 - £46,974 a year
- Full-time
- Doctoral degree
- Engineering
- Laboratory experience
Senior Research Associate in Children's Social Care
University of Bristol —Bristol
- £43,482 - £50,253 a year
- Part-time
- Project management
- Contracts
- School
13d
Senior Research Associate in Logic and Programming Languages for AI Safety
University of Bristol —Bristol
- £43,482 - £50,253 a year
- Full-time
- Doctoral degree
- Analysis skills
- School
5d

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This study will add to knowledge by describing the child harm system as a whole, identifying the data sources that allow description and monitoring of that…
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Candidates must hold a valid driving licence and have appropriate business use car insurance in place. Valid UK driving licence and sole use of a car.
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research associate jobs near tormarton, gls

Clinical Research Associate, South West England

IQVIA -
Bath

Apply Now

Job details

Full-time

Qualifications

Clinical research
Maintenance

Full job description

Bath, United Kingdom | Full time | Field-based | R1550620

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 West 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 2 years 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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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research associate jobs in tormarton, gls

Clinical Research Associate, South West England