Law associate Work, Jobs in Reading, Eng (with Salaries)

Experienced Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Clinical Research Associate II, Oncology
IQVIA —Reading
- Full-time
Associate
HCR —Reading
- Annual leave
- Gym membership
13d
Paralegal - Personal Injury
Boyes Turner —Reading
- Hybrid work
- Microsoft Outlook
- Microsoft Office
- Communication skills
Associate Professor in Commercial Law
University of Reading —Reading
- £59,966 - £67,468 a year
- Full-time
- Doctoral degree
- Leadership
- Communication skills
1d
Associate Data Visualization Analyst
SAS —Marlow
- Computer Science
- Sales
- Data analysis skills
Investment Associate
Maven Capital Partners UK —Reading
- Full-time
- Business development
- Analysis skills
- Organisational skills
- Paid training
- Annual leave
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Associate Solicitor- Private Client Advisory- Reading
Irwin Mitchell —Reading
Junior Infrastructure Engineer (Associate)
Visa Europe Limited —Basingstoke
- Day shift
- Computer Science
- Customer service
- Engineering
Senior Paralegal - Special Educational Needs
Boyes Turner —Reading
- 8 hour shift
- Hybrid work
- Microsoft Excel
- Customer service
- Microsoft Office
- Work from home
HR, Payroll & Benefits Administrator
Eque2 —Maidenhead
- Hybrid work
- Microsoft Excel
- Management
- Analysis skills
Training and Knowledge Lawyer
Boyes Turner —Reading
- 8 hour shift
- Hybrid work
- Business development
- Communication skills
- Marketing
Associate
Mills & Reeve LLP —Oxford
- Time management
Associate
DMH Stallard —Guildford
- Hybrid work
- Microsoft Outlook
- IT
- Construction
- Employee assistance programme
- Employee discount
13d
Application Analyst- (Associate Level)
Visa Europe Limited —Basingstoke
- 12 hour shift
- Microsoft Office
- Master's degree
- SQL
Senior Associate - Private Client
Boyes Turner —Reading
- 8 hour shift
- Hybrid work
- Business development
- Analysis skills
- Supervising experience
Solicitor - Personal Injury (3-5 years PQE)
Boyes Turner —Reading
- 8 hour shift
- Hybrid work
- Business development
- Continuous improvement
- Communication skills
Associate Sys Admin - Compute
Visa Europe Limited —Basingstoke
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
19h
Senior Associate or Principal Associate
Mills & Reeve LLP —Oxford
- Supervising experience

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Experienced Clinical Research Associate

IQVIA -
Reading

Apply Now

Job details

Full-time

Qualifications

Clinical research
Project implementation

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 in the UK.

Why IQVIA?

We share a passion for the work we do, and the impact it has on customers and patients
We are innovative, curious, and feel empowered to explore new ideas and ways of working
We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise
We are committed to growth, always learning, and making the most of agile career opportunities

Awards

IQVIA is a 2026 "Glassdoor Best Place to Work in the UK"
IQVIA is recognised as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)

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

Experience 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

Please note - this role is not eligible for UK 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

law associate jobs in reading, eng

Experienced Clinical Research Associate

Clinical Research Associate II, Oncology

Associate

Paralegal - Personal Injury

Associate Professor in Commercial Law

Associate Data Visualization Analyst

Investment Associate

Senior Clinical Research Associate

Associate Solicitor- Private Client Advisory- Reading

Junior Infrastructure Engineer (Associate)

Senior Paralegal - Special Educational Needs

HR, Payroll & Benefits Administrator

Training and Knowledge Lawyer

Associate

Associate

Application Analyst- (Associate Level)

Senior Associate - Private Client

Solicitor - Personal Injury (3-5 years PQE)

Associate Sys Admin - Compute

Senior Associate or Principal Associate

I want to receive the latest job alerts for law associate in reading, eng

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