Dan Crawford is in the pharmaceutical industry for 25 years in both large Pharma and CROs. He has spent fifteen years in Data Management where he managed or had oversight on more than 325 clinical trials. He specializes in authoring and presenting educational materials to the CDM industry, so you can look forward to highly structured, organized and educational workshop. He provided training and consulting on the implementation of standards and submission of NDA/BLA to the FDA. He’s a core team member of CDASH, and Expanded Leadership Team. He actively participates in authoring and presenting educational materials to the industry. In his current role at Veeva as Senior Director of CDMS Strategy, he is responsible for helping customers implement Veeva EDC, CDB and create best practices.

Dan Crawford
Speciality
Senior Director, Vault CDMS, Veeva SystemsDan Crawford
Senior Director, Vault CDMS, Veeva Systems

Dan Crawford is in the pharmaceutical industry for 25 years in both large Pharma and CROs. He has spent fifteen years in Data Management where he managed or had oversight on more than 325 clinical trials. He specializes in authoring and presenting educational materials to the CDM industry, so you can look forward to highly structured, organized and educational workshop.
He provided training and consulting on the implementation of standards and submission of NDA/BLA to the FDA. He’s a core team member of CDASH, and Expanded Leadership Team. He actively participates in authoring and presenting educational materials to the industry. In his current role at Veeva as Senior Director of CDMS Strategy, he is responsible for helping customers implement Veeva EDC, CDB and create best practices.