Clinical Trials Document Specialist Ii
By Fred Hutch At Seattle, WA, United States
Minimum 3 years of document management experience.
5+ years of document management experience
Experience working with clinical electronic databases, preferably Medidata Rave
Experience in organizing documents for internal and external audits
Facilitate the design and development of data collection forms, instructions and procedures.
Develop and maintain flow diagrams developed to document coding processes around eligibility and randomization.