Senior clinical research Work, Jobs in Hermitage, Brk (with Salaries)

Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Senior Clinical Trial Manager - PARTNERS Trial
University of Oxford —Oxford
- £49,119 - £63,489 a year
- Weekend availability
- Leadership
14d
Research Assistant
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Full-time
- Laboratory experience
- Bachelor's degree
3d
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
Senior Research Scientist I - Infectious Diseases
Immunocore —Oxford
- Full-time
- Doctoral degree
- Master's degree
- Presentation skills
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Nursing
- Travel
- Communication skills
- Employee assistance programme
Patient Safety and Pharmacovigilance Officer
Sanofi —Reading
- Hybrid work
- Word processing
- Communication skills
- Nursing
1h
RWE Clinical Project Manager – Oncology (FSP)
IQVIA —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- Continuous improvement
17h
Cancer Delivery and Performance Lead
Oxford University Hospitals NHS Foundation Trust —Oxford
- £79,504 - £91,609 a year
- Full-time
4d
Principal Medical Writer
ICON Plc —Reading
- Full-time
- Remote
- Bachelor's degree
- Communication skills
- Employee assistance programme
8d
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
Senior Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
10d
Director Clinical Operations, Clinical Project Managers
IQVIA —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
10d
Biomarker Specialist
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Weekend availability
- Laboratory experience
- Master's degree
- Bachelor's degree
Clinical Trial Assistant - Clinical Supplies
ICON Plc —Reading
- Full-time
- Remote
- Data analysis skills
- Bachelor's degree
- Communication skills
- Employee assistance programme
8d
Senior or Principal Medical Writer
ICON Plc —Reading
- Full-time
- Remote
- Communication skills
- Employee assistance programme
Clinical Research Fellow in Translational Myeloma Research
University of Oxford —Oxford
- £38,831 - £52,656 a year
- Full-time
- Doctoral degree
- Bachelor's degree
- Annual leave
4d
Senior Therapy Assistant
Oxford University Hospitals NHS Foundation Trust —Oxford
- £28,392 - £31,157 a year
- Part-time
- Organisational skills
- Hospice
7d
Senior Vascular Scientist
Oxford University Hospitals NHS Foundation Trust —Oxford
- £49,387 - £56,515 a year
- Full-time
4d
Senior Quality Assurance Manager (Clinical)
Bio Pharma Resourcing —Thames Valley
- £35,000 - £40,000 a year
- Travel
- Computer skills

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Senior Clinical Research Associate

IQVIA -
Reading

Apply Now

Job details

Full-time

Qualifications

Clinical research

Full job description

Reading, United Kingdom | Full time | Field-based | R1510425

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 hermitage, brk

Senior Clinical Research Associate

Senior Clinical Trial Manager - PARTNERS Trial

Research Assistant

Senior Clinical Technology Specialist

Senior Research Scientist I - Infectious Diseases

Clinical Research Associate

Patient Safety and Pharmacovigilance Officer

RWE Clinical Project Manager – Oncology (FSP)

Cancer Delivery and Performance Lead

Principal Medical Writer

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

Senior Clinical Trial Associate

Director Clinical Operations, Clinical Project Managers

Biomarker Specialist

Clinical Trial Assistant - Clinical Supplies

Senior or Principal Medical Writer

Clinical Research Fellow in Translational Myeloma Research

Senior Therapy Assistant

Senior Vascular Scientist

Senior Quality Assurance Manager (Clinical)

I want to receive the latest job alerts for senior clinical research in hermitage, brk

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