I've been in the pharmaceutical industry for more than 25 years in both large Pharma and CROs. I spent fifteen years in Data Management where I managed or had oversight on more than 325 clinical trials. I provided training and consulting on the implementation of standards and submission of NDA/BLA to the FDA. I'm a core team member of CDASH and Expanded Leadership Team. I actively participate in authoring and presenting educational materials to the industry. In my current role at Veeva, I am responsible for helping customers implement Veeva EDC, CDB and create best practices.