research associate Work, Jobs in arborfield (with Salaries)

Experienced Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Clinical Research Associate II, Oncology
IQVIA —Reading
- Full-time
Postdoctoral Research Assistant
University of Reading —Reading
- £36,636 - £46,049 a year
- Full-time
- Doctoral degree
- University
- Python
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Nursing
- Travel
- Communication skills
- Employee assistance programme
Research Assistant in Nutritional Sciences
University of Surrey —Guildford
- £34,610 - £36,636 a year
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- University
- Relocation assistance
3d
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Research Fellow - CoSTAR National Lab
University of Surrey —Guildford
- £37,694 - £46,049 a year
- Full-time
- Hybrid work
- Doctoral degree
- University
- School
- Relocation assistance
Research Integrity Associate
Taylor and Francis —Abingdon
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Organisational skills
- Work from home
- Employee assistance programme
Quick apply
21h
Clinical Site Associate
ICON Plc —Reading
- Full-time
- Microsoft Office
- Bachelor's degree
- Data entry
- Employee assistance programme
CRA II
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
12h
Quantum Specialist KTP Associate
University of Sussex —Middlesex
- £51,753 - £56,535 a year
- Full-time
- University
- Business
- School
13d
Associate Director - Ecology
AECOM —Basingstoke
- Full-time
- Hybrid work
Sr. CTM Associate
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Travel
- In-person
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- Negotiation
Associate Biostatistics Director - FSP (Permanent Home-based)
IQVIA —Reading
- Full-time
- Remote
- Doctoral degree
- Data analysis skills
- Leadership
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree

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Clinical Research Associate II, Oncology
IQVIA —Reading
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. May support start-up phase.
Clinical Research Associate
ICON Plc —Reading
Experience across both investigational product (IP) and medical device trials is highly desirable. Expertise in site monitoring, data integrity, and risk-based…

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research associate jobs near arborfield

Experienced Clinical Research Associate

IQVIA -
Reading

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Job details

Full-time

Qualifications

Clinical research
Project implementation

Full job description

Reading, United Kingdom | Full time | Field-based | R1521358

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 the UK.

Why IQVIA?

We share a passion for the work we do, and the impact it has on customers and patients
We are innovative, curious, and feel empowered to explore new ideas and ways of working
We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise
We are committed to growth, always learning, and making the most of agile career opportunities

Awards

IQVIA is a 2026 "Glassdoor Best Place to Work in the UK"
IQVIA is recognised as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)

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

Experience of independent on-site monitoring
You have successfully managed multiple clinical trial protocols across diverse investigative sites.
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Life science degree educated or equivalent industry experience
Flexibility to travel to sites

Please note - this role is not eligible for UK 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

research associate jobs in arborfield

Experienced Clinical Research Associate

Clinical Research Associate II, Oncology

Postdoctoral Research Assistant

Clinical Research Associate

Research Assistant in Nutritional Sciences

Specialist, R&D Contracts & Business Operations

Senior Clinical Research Associate

Research Fellow - CoSTAR National Lab

Research Integrity Associate

Clinical Site Associate

CRA II

CRA

Patient Recruitment Associate II

Quantum Specialist KTP Associate

Associate Director - Ecology

Sr. CTM Associate

Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

Associate Biostatistics Director - FSP (Permanent Home-based)

Clinical Trials Manager

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