Industry Experience

Consultant to Legal Division

Warner Chilcott (now Allergan)

Manager, Pharmaceutical Licensing & Business Development

Warner-Lambert Company (now Pfizer)

Legal Advisor, Legal Division

Warner-Lambert Company (now Pfizer)

Linda has over twenty years of experience drafting, negotiating and managing specialized contracts in the biopharmaceutical industry, including agreements for preclinical and clinical studies, research collaborations, master services and consulting, and other agreements relating to the development, manufacturing and testing of drug compounds. Linda focuses much of her work on handling clinical trial agreements for large multi-center studies, both in the U.S. and in other countries.

experience +

experience –

Warner Chilcott (now Allergan)

Consultant to Legal Division

  • Drafted and negotiated various agreements relating to the pharmaceutical industry

Warner-Lambert Company (now Pfizer)

Manager, Pharmaceutical Licensing & Business Development

  • Evaluated licensing opportunities
  • Assisted in structuring business deals

Legal Advisor, Corporate Legal Division

  • Responsible for a broad range of agreements relating to research and drug development activities

Recent Client Work +

Recent Client WOrk –

  • Phase 2/3 gene therapy clinical trial sponsored by bluebird bio, Inc. involving approximately 12 subjects across 5 sites in the US, France and the UK
  • Phase 3 clinical trial sponsored by Tesaro, Inc. involving approximately 300 subjects across multiple sites in the US, Canada and Europe
  • Phase 1b/2 clinical trial sponsored by aTyr Pharma, Inc. involving approximately 44 subjects across 6 sites in the US and Europe

Community +

Community –

  • Model Agreements & Guidelines International (MAGI), member
Education
  • ‍Fairleigh Dickinson University, M.B.A.
  • Thomas Edison State University, B.S., Business Administration
  • ‍RKD Paralegal Studies, Inc., Paralegal Certificate