Research operations occupations Work, Jobs in Sonning, Brk (with Salaries)

Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
- Recruiting
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- Full-time
- No degree
- Travel
- Recruiting
13d
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Clinical Research Trials Assistant
University of Oxford —Oxford
- £32,108 - £37,338 a year
- Full-time
- Microsoft Word
- Doctoral degree
- University
- Annual leave
11d
Research Support Administrator
Buckinghamshire New University —High Wycombe
- £26,093 - £28,778 a year
- Hybrid work
- Customer service
- University
- Organisational skills
- Employee discount
13d
Clinical Research Associate 1
ICON Plc —Reading
- Full-time
- Laboratory experience
- English
- Bachelor's degree
- Employee assistance programme
3d
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Part-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
Quick apply
Data Acquisition Specialist - External Data (Remote - UK)
IQVIA —Reading
- Full-time
- Remote
- Computer Science
- English
- Bachelor's degree
- Work from home
5d
Research and Development Specialist
Tecna —Farnborough
- Up to £50,000 a year
- Full-time
- Hybrid work
- Data analysis skills
- Microsoft Office
- Project management
Quick apply
14d
Research Facilitator
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Full-time
- Annual leave
11d
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
Research Assistant ARIADNE
University of Oxford —Oxford
- £35,681 - £37,338 a year
- Full-time
- Annual leave
Data Team Lead
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Mentoring
- Leadership
- Work from home
4d
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
Impact Evidence & Evaluation Officer - Internal Applicants only
Oxford Brookes University —Headington
- £32,080 - £34,610 a year
- Part-time
- Hybrid work
- Writing skills
- University
- No degree
- Annual leave
5d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
Clinical Research Administator
University of Oxford —Oxford
- £32,108 - £40,514 a year
- Full-time
- Oracle
- Administrative experience
- Organisational skills
Senior Manager, Clinical Operations - FSP Resource & Vendor Management
CSL Behring —Maidenhead
- £170,000 - £201,000 a year
- Full-time
- Master's degree
- Bachelor's degree
6d
Oxford Climate Research Network (OCRN) Coordinator
University of Oxford —Oxford
- £35,681 - £38,366 a year
- Part-time
- Social media management
- University
- Organisational skills
18h

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research operations occupations jobs near sonning, brk

Clinical Research Associate II

IQVIA -
Reading

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Job details

Full-time

Qualifications

Clinical research
Stakeholder liaison
Filing
Recruiting
Clinical compliance monitoring
Good Clinical Practice (GCP)
Good Clinical Practice (ICH-GCP) guidelines
Research participant recruitment coordination

Full job description

Reading, United Kingdom | Full time | Field-based | R1521358

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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

research operations occupations jobs in sonning, brk

Clinical Research Associate II

Clinical Research Associate - IQVIA Biotech

Specialist, R&D Contracts & Business Operations

Clinical Trial Associate

Clinical Research Trials Assistant

Research Support Administrator

Clinical Research Associate 1

Clinical Research Scientist

Data Acquisition Specialist - External Data (Remote - UK)

Research and Development Specialist

Research Facilitator

Clinical Research Associate I

Research Assistant ARIADNE

Data Team Lead

Senior CRA

Impact Evidence & Evaluation Officer - Internal Applicants only

CRA

Clinical Research Administator

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Oxford Climate Research Network (OCRN) Coordinator

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