Clinical Research Associate II, Oncology in Bolton

Bolton Full-Time 40000 - 50000 £ / year (est.) No working from home possible

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At a Glance

Tasks: Conduct site monitoring visits and manage study progress in compliance with GCP and ICH guidelines.
Company: IQVIA is a leading global provider of clinical research services and healthcare intelligence.
Benefits: Enjoy flexible working, well-being support, and career development opportunities through mentorship and internal talent marketplace.
Other info: This position is not eligible for visa sponsorship.
Why this job: Join a top-rated workplace recognised by Glassdoor and Fortune for its commitment to employee growth.
Qualifications: Requires at least 2 years of on-site monitoring experience and a degree in a scientific discipline or healthcare.

The predicted salary is between 40000 - 50000 £ per year.

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA’s Site Management (full service / multi-sponsor) team is growing and seeking experienced Clinical Research Associates across the UK & Ireland.

Why IQVIA?

Genuine 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 driving license and access to vehicle required for travel to sites

Please note - this position is not eligible for visa sponsorship. Apply today and forge a career with greater purpose, make an impact, and never stop learning!