Senior clinical trial Work, Jobs in Chalgrove, Oxf (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
7d
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
4d
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
Senior Administrator
University of Oxford —Oxford
- £35,681 - £45,212 a year
- Full-time
- Remote
- Administrative experience
- IT
Senior Product Manager (Pharma Clinical Trials)
Perspectum —Oxford
- £65,000 - £75,000 a year
- Full-time
- Marketing
- Presentation skills
- Bachelor's degree
Quick apply
Biomarker Specialist
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Weekend availability
- Laboratory experience
- Master's degree
- Bachelor's degree
12d
Senior Quality Assurance Manager (Clinical)
Bio Pharma Resourcing —Thames Valley
- £35,000 - £40,000 a year
- Travel
- Computer skills
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Senior Clinical Trials Pharmacy Assistant
Oxford University Hospitals NHS Foundation Trust —Oxford
- £25,760 - £27,476 a year
- Weekend availability
14d
Project Manager
Theolytics —Oxford
- Organisational skills
- IT
- Communication skills
- Flexible schedule
Senior Clinical Research Nurse
Frimley Health NHS Foundation Trust —Slough
- £41,957 - £50,387 a year
- Full-time
- Leadership
18h
Senior CRA
Fortrea —Maidenhead
- Full-time
- Communication skills
Senior Director, Global Clinical Program Lead, Immunoglobulin
CSL Behring —Maidenhead
- £338,000 - £400,000 a year
- Full-time
Dedicated Line Manager - Clinical Project Management
IQVIA —Reading
- Full-time
- Remote
- Management
- Customer service
- Microsoft Office
Clinical Data Management Lead, home-based
IQVIA —Reading
- Full-time
- Remote
- Anatomy knowledge
- Customer service
- Project management
Project & Operations Manager
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Full-time
- Doctoral degree
- Project management
- University
- Annual leave
9d
Biomedical Scientist / Specialist Biomedical Scientist
Deciphex —Oxford
- 8 hour shift
- Laboratory experience
- English
- Mentoring
- Annual leave
Quick apply
Medical Writing Manager – Patient Centered Solutions, Strategic & Scientific Research
IQVIA —Reading
- Full-time
- Microsoft Office
- Bachelor's degree
- Medical terminology
Clinical Data Management Lead
IQVIA —Reading
- Full-time
- Remote
- Oracle
- Bachelor's degree
- Leadership
- Work from home

I want to receive the latest job alerts for senior clinical trial in chalgrove, oxf

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

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 | R1540017

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?

Genuine 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 3-5 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

senior clinical trial jobs in chalgrove, oxf

Senior Clinical Research Associate

Senior Clinical Trial Manager - PARTNERS Trial

Senior Clinical Trial Administrator

Senior Clinical Technology Specialist

Senior Administrator

Senior Product Manager (Pharma Clinical Trials)

Biomarker Specialist

Senior Quality Assurance Manager (Clinical)

Sr. Clinical Project Manager (Europe)

Senior Clinical Trials Pharmacy Assistant

Project Manager

Senior Clinical Research Nurse

Senior CRA

Senior Director, Global Clinical Program Lead, Immunoglobulin

Dedicated Line Manager - Clinical Project Management

Clinical Data Management Lead, home-based

Project & Operations Manager

Biomedical Scientist / Specialist Biomedical Scientist

Medical Writing Manager – Patient Centered Solutions, Strategic & Scientific Research

Clinical Data Management Lead

I want to receive the latest job alerts for senior clinical trial in chalgrove, oxf

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected