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Provide guidance and daily oversight for the successful management of all aspects of Phase I to III and Late Phase Trials (including regulatory Post Marketing Surveillance) within designated program budgets and timelines Resolve problems using national and international regulations, guidelines, and investigator interaction Contributes to development of Request For Proposals and participates in selection and management of CROs/vendors
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At least 6+ years of experience in a clinical trial/ PMS area and a BS/ BA/ RN in a relevant scientific discipline Fluent in English Working knowledge and experience with Word, PowerPoint and Excel
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