Clinical Trial Assistant
IQVIA · Pasig, Philippines
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This role supports clinical trial operations by maintaining accurate Trial Master Files, managing clinical documentation, and coordinating Case Report Forms alongside Clinical Research Associates and regulatory teams. The position requires 3–4 years of administrative experience, preferably with at least one year in clinical research, and proficiency in standard office software and English communication.
What they're looking for
- High school diploma or equivalent
- 3-4 years of administrative support experience
- Proficiency with Microsoft Word, Excel, and PowerPoint
- Strong written and verbal English communication skills
- Effective organizational and time management abilities
- One year clinical research experience strongly preferred
- Ability to work collaboratively with diverse stakeholders
What you'll be doing
- Maintain and update Trial Master Files and clinical documents to track site compliance
- Prepare, handle, distribute, and archive clinical documentation per standard procedures
- Coordinate tracking of Case Report Forms, queries, and clinical data flow
- Serve as central contact for clinical team communications and correspondence
- Accompany Clinical Research Associates on site visits to assist with monitoring duties
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.