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Sharon Bodrug is a seasoned executive with extensive experience in program management, product development, and research and development. She has held various leadership positions at Illumina, Hologic, and Sanford-Burnham Medical Research Institute, where she has led cross-functional teams, developed and executed strategic plans, and oversaw the launch of multiple products. Sharon holds a PhD in Molecular and Medical Genetics from the University of Toronto and a BSc in Genetics from the University of Western Ontario.

Experience

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Director, R&D Program Management
      • Sep 2021 - Present

    • Associate Director Program Management
      • Sep 2014 - Sep 2021

  • Hologic
    • San Diego
    • Associate Director Program Management
      • 2007 - Aug 2014
      • San Diego

      • Led the execution of three Oncology product development projects through leadership and oversite of cross-functional core teams; resulted in CE and US IVD PMA approval of PCA3 biomarker for prostate cancer• Supported strategic discussions regarding the Oncology portfolio with resource, project cost and timeline estimates• Generated and managed project budgets• Lead cross functional team to develop multiple respiratory assays on new instrument with new consumables and manufacturing processes

    • United States
    • Biotechnology Research
    • 500 - 600 Employee
    • Senior Program Manager
      • 2005 - 2007

      • Led first Oncology biomarker (PCA3) program from research to commercial ASR launch on time and on budget• Spearheaded the strategy for clinical research studies to support Oncology biomarker PCA3• Key member of Oncology business unit that determined strategic direction including licensing of a second prostate cancer biomarker – TMPRSS2:ERG

    • Senior Staff Sceintist
      • 2002 - 2005

      • Lead effort for quantitative viral projects on TIGRIS• Technical lead and Core Team leader for new prostate biomarker, PCA3:develop dual quantitative TMA assay• Lead efforts of 8-9 scientists and technicians

    • Staff Scientist
      • 1999 - 2002

      • Lead technical efforts for feasibility studies for quantitative HIV and HCV viral load assays – incorporation of internal control, extend dynamic range, improve subtype detection• R&D technical lead and Core Team lead for quantitative HCV ASR project – launch product that is still on the market• Key member of strategy team for Viral Diagnostics program• Lead research studies with collaborators for the HIV-1 viral load assay• Lead assay integration efforts for some studies for the CT/GC on TIGRIS program• Led R&D team of 6-8 scientists and technician

    • Senior Research Scientist
      • 1996 - 1999

      • R&D technical lead and Core Team lead for quantitative HIV program• Responsible for the development efforts of the quantitative HIV-1 viral load assay• Initiate multiple research studies with collaborators for the HIV-1 viral load assay• Led R&D team of 5-6 scientists and technicians• Initiate Design Control efforts for quantitative HIV-1 program

    • Research Scientist
      • 1994 - 1996

      • Technical work and supervision of 2 technicians in the development and product improvement of assays for chlamydia trachomatis

    • Post Doctoral Fellow
      • Jun 1993 - Nov 1994
      • La Jolla, CA

      Cancer research - Role of genes involved in apoptosis

    • Post Doctoral Fellow
      • Mar 1991 - Mar 1993
      • Victoria, Australia

      Cancer research - Cell cylce regulation related to B and T cell cancer; generate transgenic mouse model

    • Research Technician
      • 1983 - 1984
      • London, Canada

Education

  • 1985 - 1991
    University of Toronto
    Doctor of Philosophy (PhD), Molecular and Medical Genetics
  • 1979 - 1983
    The University of Western Ontario
    Bachelor of Science (BSc), Genetics

Suggested Services

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Industry Focus. “Biotechnology”

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