Clinical trial Work, Jobs in Reading, Brk (with Salaries)

Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
Regulatory and Start Up Specialist - UK
IQVIA —Reading
- Full-time
- Remote
- Maintenance
- Bachelor's degree
- Referral programme
2d
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
3d
RWE Associate Clinical Project Manager – Oncology (FSP)
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
20h
Manager, Regulatory Clinical Trial Authorization (CTA)
CSL Behring —Maidenhead
- Full-time
- Customer service
- Computer literacy
- English
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Research Assistant
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Full-time
- Laboratory experience
- Organisational skills
- Communication skills
2d
Clinical Trial Program Lead
Eli Lilly —Bracknell
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
1d
Clinical Research Assistant / Clinical Research Practitioner
Oxford Health NHS Foundation Trust —Oxford
- £32,073 - £39,043 a year
- Full-time
- Annual leave
- Employee assistance programme
7d
Senior Clinical Trial Manager - PARTNERS Trial
University of Oxford —Oxford
- £49,119 - £63,489 a year
- Weekend availability
- Leadership
14d
Regulatory Science and Policy Associate - VIE Contract
Sanofi —Reading
- English
- Communication skills
1d
Senior Medical Writer (remote US-based)
Porterhouse Medical Group —Reading
- Remote
- Management
- Doctoral degree
- Master's degree
- Annual leave
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
11d
Clinical Data Management Lead, home-based
IQVIA —Reading
- Full-time
- Remote
- Anatomy knowledge
- Customer service
- Project management
Biomarker Specialist
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Weekend availability
- Laboratory experience
- Master's degree
- Bachelor's degree
Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)
IQVIA —Reading
- From £58,500 a year
- Full-time
- English
- Microsoft Office
- Bachelor's degree
Trial Manager
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Full-time
- Hybrid work
- Management
- Administrative experience
- Project management
Site Enrollment and Engagement Lead
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
Post-Trial Access Manager, Continued Access - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- No degree
- Employee assistance programme

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clinical trial jobs near reading, brk

Clinical Research Associate II

IQVIA -
Reading

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Job details

Full-time

Qualifications

Clinical research

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.

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.

Apply Now

Refine Your Search

clinical trial jobs in reading, brk

Clinical Research Associate II

Regulatory and Start Up Specialist - UK

Clinical Biospecimen Scientist - Single Sponsor Dedicated

RWE Associate Clinical Project Manager – Oncology (FSP)

Manager, Regulatory Clinical Trial Authorization (CTA)

Senior Clinical Research Associate

Research Assistant

Clinical Trial Program Lead

Clinical Research Assistant / Clinical Research Practitioner

Senior Clinical Trial Manager - PARTNERS Trial

Regulatory Science and Policy Associate - VIE Contract

Senior Medical Writer (remote US-based)

Senior Clinical Trial Administrator

Clinical Data Management Lead, home-based

Biomarker Specialist

Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)

Trial Manager

Site Enrollment and Engagement Lead

Senior Clinical Technology Specialist

Post-Trial Access Manager, Continued Access - Sponsor Dedicated

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