6 days left
- Full Time
The contractor shall have a scientific background to work directly with nonclinical study teams, research scientist, project managers and Regulatory affairs personnel to prepare complex report documents from rawand/or processed data. Specific tasks include:
- Prepare documents to include but are not limited to: Protocols and protocols amendments, research and nonclinical study reports, and FDA animal rule submission document in compliance with FDA/GLP regulations Shall manipulate data and scientific findings in appropriate table and text for presentation in logical fashion. Documents review totaling 3-6 per month.
- Will attend meeting and participate in study and project meetings to provide input regarding deliverable, timelines and processes as needed. Attends 2-4 meetings per month.