clinical trial Work, Jobs in reading, eng (with Salaries)

Experienced Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Clinical Trial Educator (Fixed-term contract for 1 year)
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
Clinical Site Associate
ICON Plc —Reading
- Full-time
- Microsoft Office
- Bachelor's degree
- Data entry
- Employee assistance programme
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Nursing
- Travel
- Annual leave
- Employee assistance programme
Manager, Regulatory Clinical Trial Authorization (CTA)
CSL Behring —Maidenhead
- Full-time
- Customer service
- Computer literacy
- English
PV Assistant
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
- Employee assistance programme
3d
Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
2d
Senior CRA
IQVIA —Reading
- Full-time
- No degree
(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay
Moderna, Inc. —Oxford
- Overtime
- Microsoft Powerpoint
- Laboratory experience
- Master's degree
- Annual leave
Senior Clinical Trial Manager - PARTNERS Trial
University of Oxford —Oxford
- £49,119 - £63,489 a year
- Weekend availability
- Leadership
2d
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Research Assistant - Ophthalmology
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Part-time
3d
Pharmaceutical Delivery Driver
LF&E Refrigerated Transport —High Wycombe
- £33,134.40 a year
- Full-time
- Customer service
- Driving
- In-person
- Employee assistance programme
Quick apply
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
2d
CRA II
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
Clinical Project Manager I
Perspectum —Oxford
- £33,000 - £45,000 a year
- Full-time
- Project management
- Communication skills
Quick apply
Clinical Research Fellow – Malaria Vaccine Programme
University of Oxford —Oxford
- £38,831 - £73,992 a year
- Full-time
- Laboratory experience
6d
Trial Manager
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Full-time
- Hybrid work
- Management
- Administrative experience
- Project management
3d
Post-Trial Access Manager, Continued Access - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- No degree
- Employee assistance programme
12d

I want to receive the latest job alerts for clinical trial in reading, eng

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical trial jobs near reading, eng

Experienced Clinical Research Associate

IQVIA -
Reading

Apply Now

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

clinical trial jobs in reading, eng

Experienced Clinical Research Associate

Clinical Trial Educator (Fixed-term contract for 1 year)

Clinical Site Associate

Clinical Research Associate

Manager, Regulatory Clinical Trial Authorization (CTA)

PV Assistant

Clinical Research Associate - 12 months' monitoring experience required

Senior CRA

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

Senior Clinical Trial Manager - PARTNERS Trial

Senior Clinical Technology Specialist

Senior Clinical Research Associate

Research Assistant - Ophthalmology

Pharmaceutical Delivery Driver

Research Facilitator

CRA II

Clinical Project Manager I

Clinical Research Fellow – Malaria Vaccine Programme

Trial Manager

Post-Trial Access Manager, Continued Access - Sponsor Dedicated

I want to receive the latest job alerts for clinical trial in reading, eng

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected