PROFESSIONAL EXPERIENCE
IMPACT CLINICAL TRIALS, Los Angeles, CA
May 2008 - Present
Regulatory Coordinator:
* Responsible for the collection of regulatory documents that are required in o
rder to open a clinical research study
* Coordinate with the 4 satellite sites to prepare the regulatory submissions fo
r all clinical research being conducted across the network
* Interface with sponsors, sites, monitors and Institutional Review Boards in or
der to expedite the submission process and throughout the course of a clinical t
rial
COMPUTER SOFTWARE
Microsoft Word, Excel, PowerPoint, Adobe Acrobat, Access, IntraLinks