Clinical associate Work, Jobs in West Berkshire, Brk (with Salaries)

Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
14d
RWE Associate Clinical Project Manager – Oncology (FSP)
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
19h
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Overseas Patients Co-ordinator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
- Administrative experience
- Communication skills
Manager - Patient Experience Data
IQVIA —Reading
- Full-time
- Remote
- Project management
- IT
- Time management
4d
Senior Associate Physiotherapist
Therapies On Thames —Newbury
- £45 - £50 an hour
- Part-time
- Anatomy knowledge
- Patient care
- Medical terminology
Quick apply
Regulatory Science and Policy Associate - VIE Contract
Sanofi —Reading
- English
- Communication skills
1d
Hospital Pharmacy Workflow Specialist - Plymouth
BD —Winnersh
- £42,000 - £64,050 a year
- Full-time
- Hybrid work
- Hospital
- Travel
- In-person
Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
2d
Clinical Post Market Surveillance Sr Specialist
Zimmer Biomet —Swindon
- Full-time
- Analysis skills
- Travel
- Health & wellbeing programme
Research Associate in Neural Rendering and Medical Image Reconstruction
University of Oxford —Oxford
- £39,424 - £43,984 a year
- Doctoral degree
- Machine learning
- In-person
- Annual leave
Associate Clinical Psychologist
Well Mind People Ltd —Wallingford
- £60 - £70 an hour
- Childcare
- Working with children
- Bachelor's degree
Quick apply
8d
Associate Occupational Therapist - Paediatrics
KT Healthcare —Oxford
- £50 - £70 an hour
- Part-time
- School
Quick apply
1d
Dental Associate PRIVATE
St Marys Dental Practice —Wallingford
- £69,148 - £200,000 a year
- Part-time
- Anatomy knowledge
- CAD
- Bachelor's degree
Quick apply
13d
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Clinical Specialist, Advanced Access - South London
BD —Winnersh
- £43,300 - £66,025 a year
- Maintenance
- Supervising experience
- Mentoring
21h
Clinical Fellow ST3+ in Stroke Medicine
Great Western Hospitals NHS Foundation Trust —Swindon
- £67,325 a year
- Full-time
- Rehabilitation centre
15h
Associate Dentist
Dentopedia Group —Dorchester
- Part-time
Quick apply
Nursing Associate
Hedena Health (Bury Knowle Health Centre) —Headington
- Part-time
- Care experience
- Nursing
- Employee discount
Quick apply
2d

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Clinical Research Associate II

IQVIA -
Reading

Apply Now

Job details

Full-time

Qualifications

Clinical research

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.

Apply Now

Refine Your Search

clinical associate jobs in west berkshire, brk

Clinical Research Associate II

Research Facilitator

RWE Associate Clinical Project Manager – Oncology (FSP)

Senior Clinical Research Associate

Overseas Patients Co-ordinator

Manager - Patient Experience Data

Senior Associate Physiotherapist

Regulatory Science and Policy Associate - VIE Contract

Hospital Pharmacy Workflow Specialist - Plymouth

Regulatory Affairs Specialist

Clinical Post Market Surveillance Sr Specialist

Research Associate in Neural Rendering and Medical Image Reconstruction

Associate Clinical Psychologist

Associate Occupational Therapist - Paediatrics

Dental Associate PRIVATE

Senior Regulatory Affairs Specialist

Clinical Specialist, Advanced Access - South London

Clinical Fellow ST3+ in Stroke Medicine

Associate Dentist

Nursing Associate

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