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    • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
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Clinical Research Associate, South West England
IQVIA
·
3.7
Bath
Full-time
Apply on company site

Job details

Pay information not provided
Full-time
Bath

Full job description

Bath, United Kingdom | Full time | Field-based | R1550620


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 South West England.

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 independent on-site monitoring experience of interventional studies
  • Experience across start-up, enrolment, maintenance, close-out
  • Digital literacy, including confidence using AI tools in a professional setting
  • Degree in scientific discipline / 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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.


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.

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