Clinical research associate Work, Jobs in New Haw, Sry (with Salaries)

Clinical Research Associate II
IQVIA —Reading
- No degree
Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Office
- Master's degree
- Annual leave
- Gym membership
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Reading
- Hybrid work
- Management
- Doctoral degree
- Data analysis skills
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
10d
CRA2 - Multi-Sponsor Department
IQVIA —Reading
- No degree
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- No degree
- Travel
2d
Consultant (Clinical Outcome Assessment - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Doctoral degree
- Annual leave
- Gym membership
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Experienced CRA - Single Sponsor Dedicated
IQVIA —Reading
- No degree
Research Associate
Imperial College London —South Kensington
- £43,863 - £57,582 a year
- Full-time
- Doctoral degree
- University
- Machine learning
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
7d
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences
University of Surrey —Guildford
- Full-time
- University
10d
Research Associate in Osteoarthritis Biostatistics
Imperial College London —Hammersmith
- £49,017 - £57,472 a year
- Full-time
- Hybrid work
- Doctoral degree
- Computer skills
- Communication skills
9d
Senior Clinical Research Associate
IQVIA —Reading
- No degree
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Senior Study Start Up Associate
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
9d
CRA II, client-dedicated (fixed-term)
Fortrea —Maidenhead
- Full-time
- Travel
- Organisational skills
- Communication skills
Associate Professor in Implementation Science for Global Eye Health
London School of Hygiene & Tropical Medicine —London
- £64,469 - £73,994 a year
- Full-time
- Hybrid work
- Doctoral degree
- Annual leave
2d

I want to receive the latest job alerts for clinical research associate in new haw, sry

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

Explore jobs in more locations

clinical research associate jobs near new haw, sry

Clinical Research Associate II

IQVIA -
Reading

Apply Now

Job details

Qualifications

Clinical research

Full job description

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 research associate jobs in new haw, sry

Clinical Research Associate II

Associate (Clinical Outcome Assessments - COA)

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Clinical Trial Associate

CRA2 - Multi-Sponsor Department

Clinical Research Associate - IQVIA Biotech

Consultant (Clinical Outcome Assessment - COA)

CRA 2 - Single Sponsor Dedicated

Experienced CRA - Single Sponsor Dedicated

Research Associate

Study Start Up Associate

Specialist, R&D Contracts & Business Operations

Sr. CRA 1 - Single Sponsor Dedicated

Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences

Research Associate in Osteoarthritis Biostatistics

Senior Clinical Research Associate

Clinical Trials Manager

Senior Study Start Up Associate

CRA II, client-dedicated (fixed-term)

Associate Professor in Implementation Science for Global Eye Health

I want to receive the latest job alerts for clinical research associate in new haw, sry

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected