Russell Weiner

Russell Weiner

About

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Biopharmaceutical Executive | VP, Translational Sciences | Biomarkers, Precision Medicine & Companion Diagnostics | Oncology & Rare Disease | Board Chair & Dire
United States

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Résumé


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  • Alexion Pharmaceuticals Inc
    VP, Head Translational Sciences
    Alexion Pharmaceuticals Inc
    Nov 2024 - Current (1 year 9 months)
  • A
    President
    American Association of Pharmaceutical Scientists AAPS
    Sep 2023 - Current (2 years 11 months)
  • Fight Cancer Global
    Governance Board Member
    Fight Cancer Global
    Aug 2023 - Current (3 years)
  • Takeda
    Head Oncology and Cell Therapy Clinical Biomarker Sciences and Operations
    Takeda
    Dec 2021 - Jul 2024 (2 years 8 months)
    Responsible for establishing and leading a global, clinical biomarker sciences and operations team supporting oncology therapeutic and cell therapy clinical development with significant efforts in Japan and China. Notably, in less than 15 months, I built a new team, hiring over 40 staff members, covering experimental pathology (discovery support), spatial-omics, digital pathology, clinical biomarkers (molecular pathology, flow cytometry, genomics, immunoassays) and clinical biomarker operations including clinical trial logistics, sample, data, and vendor management. While building this team, I managed the design, construction, and equipping of new state-of-the-are wet labs. Leveraging cutting-edge platforms to support the technologies liste
  • Aliri Bioanalysis
    Member Board of Directors
    Aliri Bioanalysis
    Aug 2021 - Mar 2025 (3 years 8 months)
  • Gates Medical Research Institute
    Head Bioanalysis, Biomarker Development and Dx
    Gates Medical Research Institute
    Jul 2018 - Dec 2021 (3 years 6 months)
    ​I joined this startup biotech to build, from the ground up, and lead a global regulated bioanalysis (PK/IMG), biomarker, diagnostics, clinical safety and central labs, sample tracking, biorepository, and bioassay operation functions, exclusively supporting Phase 1-3 clinical trials in low and middle income (LMIC) countries. This team facilitated sample analysis at external CROs, academic institutions, and local clinical labs ensuring compliance with GLP, GCLP, CAP/CLIA and/or country specific regulations and lab standards. Drawing on my experience in large pharma, I applied these skills to the non-profit sector, focusing on developing pharmaceuticals, therapeutic antibodies, and vaccines, including TB (drugs, vaccines), malaria (vaccines,
  • BioIVT
    Chair, Scientific Advisory Board
    BioIVT
    Jan 2018 - Current (8 years 7 months)
  • Daiichi Sankyo US
    Executive Director, Global Head, Bioanalytical, Biomarker Analysis and Companion Diagnostics
    Daiichi Sankyo US
    Jan 2015 - Jul 2018 (3 years 7 months)
    Responsible for building and leading a global regulated bioanalysis, biomarker and CDx team of scientists located in the US and Japan. This team provided comprehensive support across all therapeutic areas and was responsible for overseeing global clinical trial support of Phase 1-3 studies. Responsibilities included regulated bioanalysis for small molecules (PK) and biologics (PK/IMG), development and validation of biomarker assays, and sample analysis conducted at external CROs and academic institutions ensuring compliance with GLP, GCLP, CAP/CLIA and/or country specific regulations and lab standards. Additionally, this team was tasked with the development and implementation of global CDx assays and strategies for external CDx partnerships
  • BioAgilytix
    Scientific Advisory Board
    BioAgilytix
    Jan 2014 - Dec 2015 (2 years)
  • Merck
    Executive Director, Head Molecular Biomarker and Companion Diagnostics
    Merck
    Jun 2010 - Sep 2014 (4 years 4 months)
    Research focused on cloning and over-expression of functional human deoxycytidylate deaminase and rat thymidylate synthase.
  • University of Florida
    Adjunct Faculty, Department of Pharmaceutics, College of Pharmacy
    University of Florida
    Sep 2008 - Current (17 years 11 months)
  • Bristol Myers Squibb
    Group Director, Head Biomarker & Bioanalytical Sciences
    Bristol Myers Squibb
    Jan 1993 - Jun 2010 (17 years 6 months)
  • Wadsworth Center NYS Department of Health
    Post Doctoral Fellow
    Wadsworth Center NYS Department of Health
    Nov 1991 - Jan 1993 (1 year 3 months)
Education verified_user 0% verified
  • Albany Medical College
    PhD, Biochemistry
    Albany Medical College
    Jan 1986 - Dec 1991 (6 years)
    Research focused on elucidating the structure and function of human glycoprotein hormones. Experience includes Biochemistry, Immunology, protein/peptide chemistry, cell culture, production and purification of monoclonal antibodies, EIA, RIA, iodination, electrophoresis, Western blot, solid phase peptide synthesis and chromatography.
  • Stony Brook University
    BS, Biochemistry
    Stony Brook University
    Jan 1981 - Dec 1986 (6 years)
  • State University of New York at Stony Brook
    BS, Biochemistry
    State University of New York at Stony Brook
    Jan 1981 - Dec 1986 (6 years)
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