experienced clinical research Work, Jobs in basingstoke (with Salaries)

Experienced Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Clinical Research Associate II, Oncology
IQVIA —Reading
- Full-time
Research Assistant - Ophthalmology
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Part-time
3d
Virtual Key Account Manager
IQVIA —Reading
- Full-time
- Remote
- Sales
- No degree
- Negotiation
- Employee discount
10d
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Research Nurse B6
Royal Surrey NHS Foundation Trust —Guildford
- £41,957 - £50,387 a year
- Full-time
4d
Senior CRA
IQVIA —Reading
- Full-time
- No degree
Project Manager, Remote Research Clinicians
IQVIA —Reading
- Full-time
- Remote
- English
- Project management
- Bachelor's degree
5d
Sr CRA - Oncology experienced required
ICON Plc —Reading
- Full-time
- Programmable logic controllers
- Travel
- Communication skills
- Employee assistance programme
Medical Writing Manager – Patient Centered Solutions, Strategic & Scientific Research
IQVIA —Reading
- Full-time
- Microsoft Office
- Bachelor's degree
- Medical terminology
CAMHS Practitioner PiP
Hampshire and Isle of Wight Healthcare NHS Foundation Trust —Kings Worthy
- £39,959 - £48,117 a year
- Full-time
- Childcare
- Working with children
5d
Paediatric Complex Care and Transitional Flow Coordinator
Royal Surrey NHS Foundation Trust —Guildford
- £51,657 - £58,785 a year
- Full-time
- Leadership
- Nursing
10d
Family and Systemic Psychotherapist
Berkshire Healthcare NHS Foundation Trust —Reading
- £50,008 - £56,908 a year
- Full-time
- Free parking
- Annual leave
Senior Quality Assurance Manager (Clinical)
Bio Pharma Resourcing —Thames Valley
- £35,000 - £40,000 a year
- Travel
- Computer skills
Systemic Family Psychotherapist - PiP
Hampshire and Isle of Wight Healthcare NHS Foundation Trust —Kings Worthy
- £57,528 - £64,750 a year
- Part-time
- Teaching
- Nursing
5d
Territory Business Manager
IQVIA —Basingstoke
- Full-time
- Sales
- Analysis skills
- Bachelor's degree
- Annual leave
Clinical Data Management Lead
IQVIA —Reading
- Full-time
- Remote
- Oracle
- Bachelor's degree
- Leadership
- Work from home
Site Start-Up Specialist
Fortrea —Maidenhead
- Full-time
- Hybrid work
- Microsoft Office
- Communication skills
2d
Lecturer in Dietetics
University of Reading —Reading
- £47,389 - £58,225 a year
- Part-time
2d
Assistant Psychologist
Cygnet —Woking
- £29,642.55 a year
- Full-time
- Master's degree
- Psychology
- Care plans
- Employee assistance programme
2d

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experienced clinical research jobs near basingstoke

Experienced Clinical Research Associate

IQVIA -
Reading

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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

experienced clinical research jobs in basingstoke

Experienced Clinical Research Associate

Clinical Research Associate II, Oncology

Research Assistant - Ophthalmology

Virtual Key Account Manager

Senior Clinical Research Associate

Research Nurse B6

Senior CRA

Project Manager, Remote Research Clinicians

Sr CRA - Oncology experienced required

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

CAMHS Practitioner PiP

Paediatric Complex Care and Transitional Flow Coordinator

Family and Systemic Psychotherapist

Senior Quality Assurance Manager (Clinical)

Systemic Family Psychotherapist - PiP

Territory Business Manager

Clinical Data Management Lead

Site Start-Up Specialist

Lecturer in Dietetics

Assistant Psychologist

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