Research associate Work, Jobs in Lower Earley, Brk (with Salaries)

CRA2 - Multi-Sponsor Department
IQVIA —Reading
- Full-time
- Remote
- No degree
- Work from home
Research Associate in Native Ambi...
The Rosalind Franklin Institute —Harwell
- £38,500 - £39,500 a year
- Full-time
- Doctoral degree
- Leadership
- Free parking
- Annual leave
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Reading
- Full-time
- Hybrid work
- Management
- Doctoral degree
- Data analysis skills
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
8d
Research Associate in Secondary I...
The Rosalind Franklin Institute —Harwell
- £38,500 - £39,500 a year
- Full-time
- Doctoral degree
- Leadership
- Free parking
- Annual leave
Research Associate in In Vitro Mo...
The Rosalind Franklin Institute —Harwell
- £38,500 - £39,500 a year
- Weekend availability
- Doctoral degree
- Leadership
- Free parking
- Annual leave
14d
Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
11d
PDRA in Statistical Analysis of Serial Diffraction Data
Diamond Light Source —Didcot
- £41,414 - £45,510 a year
- Full-time
- Doctoral degree
- Python
- Free parking
- Annual leave
7d
Scientific Technician / Research Associate
Wild Bioscience —Milton
- Full-time
- Data analysis skills
- Laboratory experience
- Master's degree
Quick apply
8d
Field Trials Specialist
Wild Bioscience —Abingdon
- Full-time
- Hybrid work
- Data analysis skills
- Travel
- In-person
Quick apply
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Scientist, Analytical
MedPharm —Guildford
- Full-time
- Computer literacy
- Laboratory experience
- Microsoft Office
Quick apply
9d
Experienced CRA - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- No degree
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- Full-time
- No degree
- Travel
3d
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
9d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
14d
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
11d
Assistant Forensic technician
University of Surrey —Guildford
- £14,016 - £16,040 a year
- Part-time
- Hybrid work
- University
- Relocation assistance

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CRA2 - Multi-Sponsor Department

IQVIA -
Reading

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Clinical research
Project implementation

Full job description

Reading, United Kingdom | Full time | Home-based | R1530767

IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

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

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

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

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 associate jobs in lower earley, brk

CRA2 - Multi-Sponsor Department

Research Associate in Native Ambi...

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Study Start Up Associate

Research Associate in Secondary I...

Research Associate in In Vitro Mo...

Clinical Research Associate II

Clinical Trial Associate

PDRA in Statistical Analysis of Serial Diffraction Data

Scientific Technician / Research Associate

Field Trials Specialist

CRA 2 - Single Sponsor Dedicated

Associate Scientist, Analytical

Experienced CRA - Single Sponsor Dedicated

Clinical Research Associate - IQVIA Biotech

Specialist, R&D Contracts & Business Operations

Local Study Associate Director

CRA

Senior CRA

Assistant Forensic technician

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