Brian Herbert

Paralegal at Marks, O'Neill, O'Brien, Doherty & Kelly, P.C.
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Contact Information
us****@****om
(386) 825-5501
Location
Townsend, Delaware, United States, US

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Bio

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Experience

    • United States
    • Legal Services
    • 100 - 200 Employee
    • Paralegal
      • Jul 2019 - Present

    • Owner
      • Sep 2008 - Present

      Providing Synthetic and Medicinal Chemistry services, Patent writing, Office Action/Written Opinion/Expert Witness assistance, Clinical Document Management assistance, and Private Tutoring services. Client List: Millen, White, Zelano, and Branigan, P.C. (Arlington, VA) May 2011-Present Influmedix (Radnor, PA) Feb. 2010-2011 Hoffman-La Roche Pharmaceuticals (Nutley, NJ) Aug. 2009-Feb. 2010 Memory Pharmaceuticals (Montvale, NJ) Sep. 2008-July, 2009 Providing Synthetic and Medicinal Chemistry services, Patent writing, Office Action/Written Opinion/Expert Witness assistance, Clinical Document Management assistance, and Private Tutoring services. Client List: Millen, White, Zelano, and Branigan, P.C. (Arlington, VA) May 2011-Present Influmedix (Radnor, PA) Feb. 2010-2011 Hoffman-La Roche Pharmaceuticals (Nutley, NJ) Aug. 2009-Feb. 2010 Memory Pharmaceuticals (Montvale, NJ) Sep. 2008-July, 2009

    • United States
    • Legal Services
    • Paralegal
      • Jun 2018 - Mar 2019

    • 1 - 100 Employee
    • Paralegal
      • Aug 2014 - Jun 2018

    • United States
    • Biotechnology Research
    • 1 - 100 Employee
    • Contractor- Clinical
      • Dec 2010 - Aug 2012

      • Reviewed Regulatory filings of Pre-Clinical documents. • Performed audits of Trial Master File documents at CROs to assure orderly documentation. • Prepared documents for inspection during mock FDA audits. • Reviewed and bookmarked Case Report Form (CRF) files. • Identified, coded, and filed CRO clinical documents into the NPS Trial Master File system. - Phase I, II, and III trial documents. - Investigator and General. • Reviewed Regulatory filings of Pre-Clinical documents. • Performed audits of Trial Master File documents at CROs to assure orderly documentation. • Prepared documents for inspection during mock FDA audits. • Reviewed and bookmarked Case Report Form (CRF) files. • Identified, coded, and filed CRO clinical documents into the NPS Trial Master File system. - Phase I, II, and III trial documents. - Investigator and General.

    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Senior Staff Scientist
      • Jan 2001 - Sep 2008

    • Senior Scientist
      • Feb 2000 - Dec 2000

    • Intramural Research Trainee
      • Apr 1998 - Feb 2000

      Advisor: Dr. Kenneth L. Kirk, Laboratory of Bioorganic Chemistry, NIDDK Advisor: Dr. Kenneth L. Kirk, Laboratory of Bioorganic Chemistry, NIDDK

    • United States
    • Higher Education
    • 700 & Above Employee
    • Postdoctoral Research Associate
      • May 1995 - Mar 1998

      Advisor: Professor Scott E. Denmark Advisor: Professor Scott E. Denmark

Education

  • Fairleigh Dickinson University-College at Florham
    Paralegal Studies Certificate, Paralegal Studies Program (ABA approved)
    2013 - 2013
  • PRG Winning Patents Workshop
    2012 - 2012
  • PRG Patent Bar Review Course
    2011 - 2011
  • Imperial College London
    Chemistry
    1993 - 1995
  • Colorado State University
    Ph.D. (1995), Chemistry
    1990 - 1992
  • Northwestern University
    M.S., Chemistry
    1989 - 1990
  • Saint Andrews Presbyterian College
    B.S., Biology, Math, and Chemistry
    1985 - 1989

Community

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