Senior clinical research Work, Jobs in Reading, Eng (with Salaries)

Senior Clinical Research Associate
IQVIA —Reading
- No degree
Senior Research Associate, Clinical Biomarker Laboratory, Immunoassays
Moderna, Inc. —Oxford
- Overtime
- Microsoft Powerpoint
- Laboratory experience
- Master's degree
- Annual leave
Senior Research Associate, Bioanalytical & Molecular Assays
Moderna, Inc. —Oxford
- Full-time
- Data analysis skills
- Bachelor's degree
- Annual leave
Senior Quality Assurance Manager (Clinical)
Bio Pharma Resourcing —Thames Valley
- £35,000 - £40,000 a year
- Travel
- Computer skills
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
1d
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Senior Counsellor
University of Oxford —Oxford
- £49,119 - £58,265 a year
- Hybrid work
- Supervising experience
- University
- Annual leave
- Employee assistance programme
4h
Senior Clinical Trainer
HCRG Care Group —Farnham
- £39,959 - £48,117 a year
- Supervising experience
- Project management
- Education
- Employee discount
Quick apply
20h
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Senior Medical Writer
IQVIA —Reading
- Doctoral degree
- Computer literacy
- Master's degree
8d
Clinical Research Fellow in Gastroenterology
University of Oxford —Oxford
- £38,831 - £73,992 a year
- Full-time
- Bachelor's degree
- Organisational skills
- Annual leave
7d
Senior Research Scientist I - Infectious Diseases
Immunocore —Oxford
- Full-time
- Doctoral degree
- Master's degree
- Presentation skills
Research & Innovation Assistant
University of Oxford —Oxford
- £35,681 - £45,212 a year
- Full-time
- Administrative experience
- Maths
- Machine learning
5d
Clinical Trial Manager
University of Oxford —Oxford
- £39,424 - £51,983 a year
- Full-time
- Computer literacy
- No degree
Senior Study Startup Specialist
PSI CRO —Oxford
- Full-time
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
Quick apply
10d
Senior Clinical Specimen Acquisition Specialist
Leica Biosystems —Amersham
- Full-time
- Remote
- Doctoral degree
- Organisational skills
- Annual leave
5d
Part-Time Senior Clinical/Forensic Psychologist
Elysium Healthcare —Thatcham
- Up to £57,000 a year
- Full-time
- Care plans
- Free parking
- Annual leave
Quick apply
7d
Senior Healthcare Global Product Manager Ostomy
Hollister Europe Limited —Winnersh
- £51,282 - £80,585 a year
- Microsoft Powerpoint
- Marketing
- English
- Annual leave
- Employee assistance programme
Senior Director, Drug Development
IQVIA —Reading
- Remote
- Microsoft Powerpoint
- Master's degree
- Analysis skills
8d
Clinical Trials Coordinator
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Full-time
- Management
4d

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senior clinical research jobs near reading, eng

Senior Clinical Research Associate

IQVIA -
Reading

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Job details

Qualifications

Clinical research

Full job description

Join Us on Our Mission to Drive Healthcare Forward

IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.

With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.

Why IQVIA?

IQVIA is recognized as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list for the fifth consecutive year!
We offer genuine career development opportunities for those who want to grow as part of the organization.
The chance to work on cutting edge medicines at the forefront of new medicines development.
IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical 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

A minimum of 18 months 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

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

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

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

senior clinical research jobs in reading, eng

Senior Clinical Research Associate

Senior Research Associate, Clinical Biomarker Laboratory, Immunoassays

Senior Research Associate, Bioanalytical & Molecular Assays

Senior Quality Assurance Manager (Clinical)

Senior CRA

Sr. Clinical Project Manager (Europe)

Senior Counsellor

Senior Clinical Trainer

Senior Clinical Programmer I

Senior Medical Writer

Clinical Research Fellow in Gastroenterology

Senior Research Scientist I - Infectious Diseases

Research & Innovation Assistant

Clinical Trial Manager

Senior Study Startup Specialist

Senior Clinical Specimen Acquisition Specialist

Part-Time Senior Clinical/Forensic Psychologist

Senior Healthcare Global Product Manager Ostomy

Senior Director, Drug Development

Clinical Trials Coordinator

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