Clinical Trial Administrator - Etmf Specialist
IQVIA · Parma, Provincia di Parma
📍 On-site📅 4 Jun 2026
Job Description
Clinical Trial Administrator - eTMF Specialist
Company: IQVIA Location: Parma, Provincia di Parma Work Model: Onsite Contract Type: Contract
IQVIA is seeking an experienced e-TMF Specialist for the Supply section to join an exciting and dynamic working environment on behalf of our client, a global pharmaceutical company.
About the Role
This role is crucial for ensuring the quality and integrity of electronic Trial Master File (eTMF) documentation within clinical trials. You will be responsible for managing and maintaining the eTMF system, focusing specifically on the Investigational Products and Clinical Trial Supply sections.
Key Responsibilities
- Review eTMF plans.
- Upload documents into the eTMF system.
- Perform ongoing quality control of the eTMF, specifically for the Investigational Products and Clinical Trial Supply sections, utilizing the Company System.
- Monitor eTMF quality issues and follow up with relevant internal functions, Contract Manufacturing Organizations (CMOs), and Contract Research Organizations (CROs) until resolution.
Requirements
- Proven experience with eTMF systems.
- Solid understanding of Clinical Trial processes.
- Experience in Document Management.
- Proficiency in Quality Control procedures.
- Familiarity with the Pharmaceutical industry.
✨ This description was enhanced by AI based on the original listing.