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, work with passionate teams, and enjoy continuous learning opportunities.
- Other info: Ad-hoc travel required; not eligible for UK visa sponsorship.
- Why this job: Make a real impact on patient outcomes while developing your career in a dynamic environment.
- Qualifications: Experience in clinical trials and a degree in life sciences preferred.
The predicted salary is between 40500 - 49500 £ 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.
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.
Clinical Trials Assistant employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
