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RssRegulatory Submissions - Document Management

Accomplished Pharmaceutical Professional with 10+ years of experience in regulatory submissions, document management, and project management positions. Record of success in developing and maintaining business solutions that guarantee compliance with international regulatory guidance. Recognized for ability to identify, learn, and effectively utilize emerging technologies to provide innovative business solutions. Exceptional ability to interpret business problems, manage projects, create effective solutions, and provide training and coaching for team members. Proficient in a variety of document management databases, including daily use of Documentum products from 2002 through 2014.

Clinical Regulatory Affairs

About Me

Industry:

Science & Biotech

Occupation:

Clinical Regulatory Affairs
 

Education level:

Bachelor

Will Relocate:

Yes

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