Sr Clinical Trial Assistant - Study Start-Up & Regulatory - Sponsor Dedicated -
IQVIA · Lisbon, Portugal
RegulatoryFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Trial Assistant position supporting Clinical Research Associates and regulatory teams in maintaining trial documentation, managing clinical supplies, and ensuring site compliance. Based in Lisbon, Portugal, this role involves administrative coordination, file management, and potentially assisting with on-site monitoring activities.
What they're looking for
- High school diploma or equivalent
- 2+ years experience as a Clinical Trial Assistant
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Fluent in English and Portuguese, written and verbal
- Knowledge of GCP and ICH guidelines
- Strong organizational and time management abilities
What you'll be doing
- Update and maintain Trial Master Files and clinical documentation systems tracking site compliance
- Prepare, handle, and archive clinical documents and reports according to standard procedures
- Review study files for completeness and accuracy
- Coordinate tracking of Case Report Forms, queries, and clinical data flow
- Serve as central contact for clinical team communications and documentation management
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.