ConsultantCR

ConsultantCR ConsultantCR

Regulatory Affairs Specialist helping pharmaceutical companies worldwide to gain approval for their medicines in a timely and cost-effective manner with excellent organization and communication skills. Experienced in all phases of electronic and paper submission publishing, eCTD and CTD document processing, program management, legacy document processing, archiving, and document management.

06/27/2012

Address

Technology Square
Cambridge, MA
02139

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