clinical research associate Work, Jobs in reading, brk (with Salaries)

Clinical Research Associate II, Oncology
IQVIA —Reading
- Full-time
Experienced Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Clinical Research Associate II
PSI CRO —Oxford
- Full-time
- Remote
- Microsoft Office
- Bachelor's degree
- Travel
Quick apply
2d
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Clinical Site Associate
ICON Plc —Reading
- Full-time
- Microsoft Office
- Bachelor's degree
- Data entry
- Employee assistance programme
(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry
Moderna, Inc. —Oxford
- Full-time
- Laboratory experience
- Microsoft Office
- Presentation skills
- Annual leave
14d
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
13h
CRA II
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
Research Associate in Neural Rendering and Medical Image Reconstruction
University of Oxford —Oxford
- £39,424 - £43,984 a year
- Doctoral degree
- Machine learning
- In-person
- Annual leave
8d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- Negotiation
Sr. CTM Associate
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Travel
- In-person
Associate Biostatistics Director - FSP (Permanent Home-based)
IQVIA —Reading
- Full-time
- Remote
- Doctoral degree
- Data analysis skills
- Leadership

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clinical research associate jobs near reading, brk

Clinical Research Associate II, Oncology

IQVIA -
Reading

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Job details

Full-time

Qualifications

Clinical research

Full job description

Reading, United Kingdom | Full time | Field-based | R1539299

Join IQVIA on our mission to accelerate innovation for a healthier world!

IQVIA UK’s Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates.

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

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

Essential Functions

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.

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.

Qualifications

Requires at least 1 year of independent on-site monitoring experience of interventional studies in the UK.

Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).

Good therapeutic and protocol knowledge as provided in company training.

Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Please note - this role is not eligible for UK visa sponsorship

#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 II, Oncology

Experienced Clinical Research Associate