Clinical Trial Assistant (CTA) - One Sponsor Dedicated, Prague

About the role

IQVIA's Clinical Functional Service Partnership (CFSP) offers a dedicated program with a single sponsor, combining specialist expertise with the stability and career support of a global organisation. As a Clinical Trial Assistant in Prague, you will support the day-to-day running of clinical trials, learn alongside experienced CRAs and Project Managers, and build a foundation for future clinical research roles.

Key responsibilities

• Maintain and update Trial Master Files (TMF) and study documentation
• Support document preparation, filing, tracking and archiving
• Review study files for completeness and compliance
• Coordinate clinical trial supplies and tracking records
• Assist with CRF tracking, study queries and data workflows
• Act as a key contact for project communications and documentation
• Guide and mentor other Clinical Trial Assistants, supporting onboarding, training and knowledge sharing
• Serve as a subject matter expert on clinical trial processes, possibly leading CTA study teams and contributing to recruitment
• Support departmental quality and process improvement initiatives

Required profile

• Passion for clinical research and healthcare
• Science degree preferred
• Minimum 2 years of clinical trials support experience
• Strong organisation skills and attention to detail
• Ability to manage multiple priorities and meet deadlines
• Effective communication skills and ability to work collaboratively across teams