Dan Crawford

About Dan Crawford

I\'ve been in the pharmaceutical industry for 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 provide training and consulting on the implementation of standards within an FDA submission. 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 as Senior Director of CDMS Strategy, I am responsible for growing Vault CDMS in the emerging market space. I work with various teams by providing thought leadership, sales support and driving market strategy and product development.

Experience

1. Senior Director, Vault Cdms

   Veeva Systems

   Nov 2018 — Present · Radnor, PA, US

   As a Market Owner, I am responsible for growing Vault CDMS in the CRO space. I will be working with the product team to develop and grow the market by providing thought leadership, sales support and driving market strategy and product development.

Skills

• Medical Devices
• Clinical Research
• Good Clinical Practice (Gcp)
• Gcp
• Line Management
• Biotechnology
• Electronic Data Capture (Edc)
• Clinical Development
• Ich-Gcp
• 21 Cfr Part 11
• U.s. Title 21 Cfr Part 11 Regulation
• Meddra
• Cdisc Standards
• Oncology
• CRO
• CRO Management
• Clinical Trials
• U.s. Food and Drug Administration (Fda)
• Crf Design
• Edc
• Therapeutic Areas
• Ctms
• Pharmaceutical Industry
• Sop
• Fda
• Cdisc
• Computer System Validation
• Data Management
• Clinical Data Management
• Oracle Clinical
• Regulatory Submissions
• Regulatory Affairs