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Crystal Gasby has more than ten years experience in the agricultural chemical
and pharmaceutical research and development environment. She is currently
assigned to DuPont Crop Protection as a Document Administrator where she is
relied on for her skills in Microsoft Word and Documentum. Crystal provides
Document Management support to the US Registration group and works with Summary
Document Coordinators to prepare and format regulatory documents, dossiers, and
templates. In addition, she regularly contributes to the writing of a
Pharmaceutical Clinical Research & Development newsletter.
Prior to joining CPS, Crystal worked at DuPont Pharmaceuticals Co./Bristol Myers
Squibb Pharma (DPC) and held several positions from a Document Production
Specialist in the Medical Communications Group working with Clinical Research &
Development to produce FDA submission documents, to an Assistant System
Administrator in Regulatory Affairs/Drug Safety maintaining the Clintrace
database; extracting report data; developing training materials for new system
tools; and conducting new user training. |