Clinical research associate ii Work, Jobs in Headington, Oxf (with Salaries)

Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
7d

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Based on your search for clinical research associate ii

Clinical Research Associate II
IQVIA —Reading
Requires at least 2 years on-site monitoring experience of interventional studies. Ensure copies/originals (as required) site documents are available for filing…
Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Performing data review and resolution of queries to maintain…

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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

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clinical research associate ii jobs in headington, oxf

Clinical Research Associate II

Clinical Research Associate

Clinical Research Associate - 12 months' monitoring experience required

Patient Recruitment Associate II

Senior CRA

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