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Maura Buckley, CCRP

Senior Clinical Regulatory Manager

maura-buckleyMaura assists with all aspects of regulatory issues related to oncology clinical research, including interactions with network members, institutional review boards, and regulatory agencies. Regulatory services include:

  • Essential document collection and tracking
  • Initial IND (FDA) submission and maintenance of the IND
  • Distribution of updated study documents to site staff
  • Review and approval of site documents
  • Ensuring all IRB approvals are obtained by sites
  • Central IRB submissions of study materials, when applicable
  • Trial master file maintenance