At a Glance
- Tasks: Support clinical trials by managing documentation and ensuring compliance.
- Company: Join IQVIA, a leader in clinical research and healthcare innovation.
- Benefits: Gain valuable experience in a dynamic environment with growth opportunities.
- Other info: Ad-hoc travel to Maidenhead office; not eligible for UK visa sponsorship.
- Why this job: Make a real impact on patient outcomes while working with a passionate team.
- Qualifications: Experience in clinical trials and a degree in life sciences required.
The predicted salary is between 36900 - 45100 £ per year.
Join IQVIA on our mission to accelerate innovation for a healthier world!
- We are seeking a
- Clinical Trials Assistant to join our c FSP
(sponsor-dedicated) team.
This position requires candidates able to commit to ad-hoc travel sponsor's office in Maidenhead, Berkshire.
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 Power Point.
- 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.
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.
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Clinical Trials Assistant Reading employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
