At a Glance
- Tasks: Monitor clinical trials and ensure compliance with regulations while supporting study sites.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Flexible working, well-being support, and genuine career development opportunities.
- Other info: Recognised as a top workplace with excellent growth potential.
- Why this job: Make a real impact on health innovation and work with a top-rated company.
- Qualifications: 3-5 years of monitoring experience and a degree in a scientific discipline.
The predicted salary is between 40500 - 49500 £ per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s c FSP (sponsor-dedicated) team is growing and seeking Senior Clinical Research Associates.
Why IQVIA?
Genuine career development opportunities to grow as we grow Flexible working to assist work–life balance and professional success Well‑being support covering your physical, mental, and financial health
Awards
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 3-5 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.
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Senior Clinical Research Associate in Manchester employer: IQVIA LLC
IQVIA LLC is an exceptional employer located in the vibrant town of Livingston, Scotland, offering a dynamic work culture that prioritises scientific excellence and patient outcomes. Employees benefit from comprehensive training and development opportunities, fostering personal and professional growth within the clinical lab services sector. With a strong emphasis on teamwork and innovation, IQVIA provides a rewarding environment for those looking to make a meaningful impact in healthcare.
