Job Summary
A pharmaceutical research and consulting firm is filling a position for a Remote Trial Master Files Specialist II.
Must be able to:
- Support strategies, procedures, and tools for the optimization of the processes
- Recognize and consider various solutions to problems or situations
Must meet the following requirements for consideration:
- A minimum of 2 years of relevant experience in clinical research, direct eTMF experience
- General knowledge of ICH-GCP and other relevant regulations pertaining to essential documents
- Must have a general understanding of the functional area responsibilities associated with the clinical development process, trial management, and clinical trial management systems
