Clinical research associate Work, Jobs in Milton Common, Oxf (with Salaries)

Clinical Research Associate II
IQVIA —Reading
- No degree
Clinical Trials Assistant II
IQVIA —Reading
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Clinical Trials Assistant
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
9d
Site Management Associate I
PSI CRO —Oxford
- Full-time
- Hybrid work
- Customer service
- Microsoft Office
- Bachelor's degree
Quick apply
4d
Senior Clinical Research Associate
IQVIA —Reading
- No degree
Research Associate in Computational Cardiovascular Science
University of Oxford —Oxford
- £39,424 - £45,212 a year
- Doctoral degree
- Annual leave
2d
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Senior Research Fellow (Biomedical Engineering)
University of Oxford —Oxford
- £56,623 - £73,296 a year
- Full-time
- Doctoral degree
- Engineering
- Teaching
Postdoctoral Research Assistant in Bioimaging and Spatial Multiomics
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Doctoral degree
- Machine learning
- AI
Manager - Patient Experience Data
IQVIA —Reading
- Project management
- IT
- Time management
Director, Portfolio Development Process & Standards Lead
CSL Behring —Maidenhead
- £230,000 - £270,000 a year
- Full-time
- Hybrid work
- Nursing
- Master's degree
- Bachelor's degree

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Clinical Trials Assistant II
IQVIA —Reading
Key deliverables include tracking progress of the clinical trial, managing study data, budget, investigational products, mailings and correspondence and other…

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clinical research associate jobs near milton common, oxf

Clinical Research Associate II

IQVIA -
Reading

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Job details

Qualifications

Clinical research

Full job description

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.

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 on-site monitoring experience of interventional studies
Degree in scientific discipline or 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.

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clinical research associate jobs in milton common, oxf

Clinical Research Associate II

Clinical Trials Assistant II

Senior Clinical Trials Assistant

Site Management Associate I

Senior Clinical Research Associate

Research Associate in Computational Cardiovascular Science

Specialist, R&D Contracts & Business Operations

Senior Research Fellow (Biomedical Engineering)

Postdoctoral Research Assistant in Bioimaging and Spatial Multiomics

Manager - Patient Experience Data

Director, Portfolio Development Process & Standards Lead

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