Join IQVIA on our mission to accelerate innovation for a healthier world!

We are seeking a Senior Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team.

Hybrid working with 3 days per week at sponsor site in Bedfordshire, England.

Why IQVIA?

• We share a passion for the work we do, and the impact it has on customers and patients
• We are innovative, curious, and feel empowered to explore new ideas and ways of working
• We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise
• We are committed to growth, always learning, and making the most of agile career opportunities
• 2026 Glassdoor Best Place to Work in the UK
• Recognised as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)

Key Responsibilities

• Maintain and update clinical systems and documentation, including the Trial Master File.
• Support the preparation, distribution, filing, and archiving of clinical documents and reports.
• Conduct periodic reviews of study files to ensure completeness and compliance.
• Assist with clinical trial supply logistics and tracking.
• Manage Case Report Forms (CRFs), queries, and clinical data flow.
• Serve as a central point of contact for project communications and documentation.

What We’re Looking For

• Previous clinical trials support experience required.
• Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH).
• Degree in life sciences or equivalent industry experience.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Strong written and verbal communication skills in English.
• Excellent time management, organization, and collaboration skills.

Please note: This role is not eligible for UK visa sponsorship.

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

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.