Job Description

**Sr Clinical Trials Assistant, cFSP**:
**Hybrid role**
Job Overview
Leads and oversees the execution of clinical projects and research studies in accordance with global and local regulations to best meet customer needs while working toward organizational goals and strategies.
Provides project-related support to the project management teams of assigned clinical research studies. Establishes and maintains all project documentation; conducts technical reviews and audits of files for accuracy and completion; tracks key communications and documents; and maintains internal systems and databases.
Essential Functions:
Includes but not limited to:
- Support in ensuring compliance with contract, SOPs, GCPs, policies, and regulatory
- Support in meeting quality & timeline metrics
- Assist study manager/ study lead in effective management of eTMF and its Inspection Readiness
- Establishment and maintenance of Study in Gilead's Global Clinical Trials Management System...

Apply for this Position

Ready to join IQVIA? Click the button below to submit your application.

Submit Application