On behalf of our Client a global pharmaceutical company, IQVIA is looking for **a e-TMF Specialist - Supply section** who can join an exciting working environment in a dynamic atmosphere. **RESPONSIBILITIES**: - To review eTMF plans
- To upload documents in the eTMF and perform ongoing quality control of the eTMF (Investigational products and Clinical Trial Supply section) using Company System
- Monitor the eTMF quality issues and follow up with the relevant functions (internally / CMO /CRO) until their resolution.
- To provide support to eTMF users (CMOs) on the use of the system.
- Archiving of study CTS related documentation in the Company CTS repository **REQUIREMENTS AND SKILLS**: - High School and/or College Degree
- A significant experience in a similar job in the industry or CRO
- Knowledge of drug development process English knowledge
- Solid knowledge of clinical data management and
- Problem solving
- English Proficient LI-CES LI-DNP

📌 Clinical Trial Administrator (Parma)
🏢 Iqvia
📍 Parma