Clinical data Work, Jobs in Reading, Eng (with Salaries)

Experienced Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Clinical Research Associate II, Oncology
IQVIA —Reading
- Full-time
Principal Clinical Data Standards Consultant
ICON Plc —Reading
- Full-time
- Remote
- Programmable logic controllers
- Bachelor's degree
- Mentoring
- Annual leave
- Employee assistance programme
Senior CRA
IQVIA —Reading
- Full-time
- No degree
Clinical Data Management Lead, home-based
IQVIA —Reading
- Full-time
- Remote
- Anatomy knowledge
- Customer service
- Project management
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Nursing
- Travel
- Communication skills
- Employee assistance programme
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
Medical Data Reviewer
ICON Plc —Reading
- Full-time
- Nursing
- Microsoft Excel
- Doctoral degree
- Employee assistance programme
Clinical Services Manager – Wards, Day Case and Pre-Assessment
Circle Health Group —Reading
- Up to £68,500 a year
- Full-time
- Hospital
- Master's degree
- Business development
- Annual leave
- Employee discount
Clinical Site Associate
ICON Plc —Reading
- Full-time
- Microsoft Office
- Bachelor's degree
- Data entry
- Employee assistance programme
(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory
Moderna, Inc. —Oxford
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
Hospital Pharmacy Workflow Specialist - Plymouth
BD —Winnersh
- £42,000 - £64,050 a year
- Full-time
- Hybrid work
- Hospital
- Travel
- In-person
Clinical Data Management Lead
IQVIA —Reading
- Full-time
- Remote
- Oracle
- Bachelor's degree
- Leadership
- Work from home
Data Scientist
University of Oxford —Oxford
- £39,424 - £51,983 a year
- Full-time
- Data analysis skills
- Master's degree
- Analysis skills
Associate GP Dean
NHS England —Reading
- £131,827 a year
- Part-time
- No experience needed
- Annual leave
8d
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Imaging Training Specialist
ICON Plc —Reading
- Full-time
- Travel
- Organisational skills
- In-person
- Annual leave
- Employee assistance programme
Senior Clinical Coder ACC
Buckinghamshire Healthcare NHS Trust —Stoke Mandeville
- £32,073 - £39,043 a year
- Full-time
- Annual leave
14d
Research Assistant - Ophthalmology
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Part-time
16h
CRA II
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme

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clinical data jobs near reading, eng

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

clinical data jobs in reading, eng

Experienced Clinical Research Associate

Clinical Research Associate II, Oncology

Principal Clinical Data Standards Consultant

Senior CRA

Clinical Data Management Lead, home-based

Clinical Research Associate

Senior Clinical Technology Specialist

Medical Data Reviewer

Clinical Services Manager – Wards, Day Case and Pre-Assessment

Clinical Site Associate

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

Hospital Pharmacy Workflow Specialist - Plymouth

Clinical Data Management Lead

Data Scientist

Associate GP Dean

Senior Clinical Research Associate

Imaging Training Specialist

Senior Clinical Coder ACC

Research Assistant - Ophthalmology

CRA II

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