A mid-sized pharmaceutical company based in New Jersey is seeking a Global Document Management Specialist to manage Veeva Vault submissions and ensure high-quality content for medical affairs. This role requires a Master's degree and 1-3 years of experience in pharmaceutical content development. Responsibilities include managing submissions, assisting in slide kit resource development, and ensuring accuracy and compliance with guidelines. This is a 12+ month remote contract position offering healthcare benefits.
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Global Veeva Docs Specialist - Medical Affairs (Remote) in nj at Unknown Company
This position is listed as contract and able to be worked remotely.