Carl Brown

Clinical Science and Development

Role
Director, Clinical Development at Neurocrine Biosciences
Location
San Diego, CA, US
LinkedIn followers
500 followers

About Carl Brown

Scientist with experience in clinical development, regulatory affairs, and basic research. Excellent communication, writing, and presentation skills. Strengths in information gathering and dissemination, data analysis and interpretation, focusing team discussions and facilitating decisions. Ability to manage multiple projects and meet challenging timelines with high quality. Flexible and adaptive style; capable of rapidly integrating into new teams and projects.Specialties: Clinical trial protocol developmentRegulatory submissions (FDA applications)Data review, analysis, and presentation

Experience

  1. Director, Clinical Development

    Neurocrine Biosciences

    Apr 2024 — Present · San Diego, US

Education

  • Rice University

    BA, Biochemistry, Economics

    1990 — 1994

  • Baylor College of Medicine

    PhD, Molecular and Cellular Biology

    1995 — 2002

Skills

  • Diabetes
  • Project Management
  • Microsoft Office
  • Cross-Functional Team Leadership
  • Research
  • Safety Monitoring
  • Bioequivalence
  • Nda
  • Formulation
  • Pharmaceutical Industry
  • Sop
  • Fda
  • Edc
  • Clinical Research
  • Medical Writing
  • CRO Management
  • Regulatory Affairs
  • Pharmacovigilance
  • Medical Monitoring
  • Pharmacokinetics
  • Regulatory Submissions
  • Business Development
  • Cell Biology
  • Anda
  • R
  • Ich-Gcp
  • Life Sciences
  • Molecular Biology
  • Clinical Trials
  • Ind
  • Drug Discovery
  • Clinical Development
  • Oncology
  • Protocol
  • Medical Research
  • Generic Drugs
  • Regulatory Guidelines
  • Data Analysis
  • Clinical Study Design
  • Technology Transfer

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Carl Brown — Director, Clinical Development at Neurocrine Biosciences in San Diego, CA, US | Unifers