Jeff Barrus

Vice President - Head of RA/QA

Role
Vice President, Regulatory Affairs & Quality Assurance at CellCentric
Location
Cambridge, MA, US
LinkedIn followers
500 followers

About Jeff Barrus

Twenty-four years of experience in the pharmaceutical/biotechnology industry. Over twenty years in regulatory affairs & quality working in oncology, infectious disease, neurology, pain, and hematology with direct experience in the US, Canada, Europe, South America, Asia, and Oceania. Successfully managed NDA/MAA activities for assigned projects through approval. Filed several INDs and CTAs globally. Managed communication with regulatory agencies including face-to-face, telephone, and written interactions. Led preparation for and managed organization of due diligence audits with potential partners for regulatory aspects. Specialties: Regulatory strategy, quality assurance, process improvement, quality systems development, project management, regulatory publishing, electronic regulatory submissions (eCTD), database design and management

Experience

  1. Vice President, Regulatory Affairs & Quality Assurance

    CellCentric

    Apr 2025 — Present · Boston, MA, US

Education

  • University of Utah

    BS, Biology (Biochemical Engineering)

    1994 — 2000

Skills

  • Clinical Trials
  • U.s. Food and Drug Administration (Fda)
  • Pharmaceutical Industry
  • Fda
  • Clinical Development
  • Regulatory Affairs
  • Biotechnology
  • Oncology
  • Life Sciences
  • Regulatory Submissions
  • Ectd
  • Biologics
  • Ind
  • Drug Development
  • Gcp
  • Quality Assurance
  • Electronic Common Technical Document (Ectd)
  • Neurology

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Jeff Barrus — Vice President, Regulatory Affairs & Quality Assurance at CellCentric in Cambridge, MA, US | Unifers