Joanne Gibbons

Role
SVP Regulatory Affairs & Quality at Morphic Therapeutic
Location
Cambridge, MA, US
LinkedIn followers
500 followers
Manufacturing & ProductionView LinkedIn profile

About Joanne Gibbons

Seasoned pharmaceutical/biotech executive with deep expertise in all phases of drug…

Experience

  1. SVP Regulatory Affairs & Quality

    Morphic Therapeutic

    Apr 2022 — Present

Skills

  • Clinical Trial Management System (Ctms)
  • Ich-Gcp
  • Clinical Operations
  • Biotechnology
  • Clinical Study Design
  • Protocol
  • Gxp
  • Capa
  • Technology Transfer
  • Drug Development
  • CRO Management
  • Regulatory Strategy
  • Ind
  • Good Clinical Practice (Gcp)
  • Pharmacovigilance
  • Sop
  • Medical Writing
  • Ectd
  • R&D
  • Medical Affairs
  • U.s. Food and Drug Administration (Fda)
  • Vaccines
  • Regulatory Affairs
  • Fda
  • Project Management
  • Lifesciences
  • Regulatory Requirements
  • Neurology
  • Life Sciences
  • Drug Discovery
  • Oncology
  • Ctms
  • Regulatory Submissions
  • Clinical Development
  • Biologics
  • Cross-Functional Team Leadership
  • Protocol Development
  • Pharmaceutical Industry
  • Clinical Research
  • Clinical Trial Management

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Joanne Gibbons — SVP Regulatory Affairs & Quality at Morphic Therapeutic in Cambridge, MA, US | Unifers