Kickstart Your Career in Clinical Research with IQVIA!
Are you passionate about clinical research and eager to start your journey?
As a clinical intern with our site management (multi-sponsor) team, you will assist clinical trials whilst receiving comprehensive training through our development program.
We are offering a full time and paid trainee role on a 9-month fixed term contract, with the potential to become permanent upon completion.
Job Overview
• Assist with accurately updating and maintaining clinical documents and systems (e.g.,Trial Master File (TMF)) that track site compliance and performance within project timelines
• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures
• Assist with periodic review of study files for completeness
• Assist the Country Site Activation team with preparation, handling and
distribution of Clinical Trial Supplies and maintenance of tracking information
• Complete CSA training program and develop knowledge of clinical research, Good Clinical Practice (GCP) and appropriate therapeutic area and protocols
• Accompany CSAs on site visits to assist with clinical monitoring duties upon completion of required training
What We’re Looking For
• Bachelor’s degree in a scientific or healthcare discipline
• Passion for clinical research and ambition to grow into a CRA role
• Proficiency in Microsoft Word, Excel, and PowerPoint
• Strong communication skills and ability to build effective relationships
*This position 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. Learn more at
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 Research Trainee • Reading, Berkshire, United Kingdom
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