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Brenda O'Connell is a seasoned translational scientist with extensive experience in oncology, having led strategic planning and execution of translational studies at Bicara Therapeutics and Infinity Pharmaceuticals. As a Director of Translational Science at Infinity Pharmaceuticals, she spearheaded early discovery pipeline expansion efforts, managed direct and indirect reports, and presented scientific findings at conferences. Brenda holds a Doctor of Philosophy (PhD) in Cell/Cellular and Molecular Biology from Brown University, where she studied the role of c-Myc in transcription regulation. Her expertise spans biomarker analysis, regulatory interactions, and clinical operation activities, making her a valuable asset in the biopharmaceutical industry.

Experience

  • Bicara Therapeutics
    • Boston, Massachusetts, United States
    • Senior Director, Translational Science
      • Nov 2023 - Present
      • Boston, Massachusetts, United States

    • United States
    • Pharmaceutical Manufacturing
    • 300 - 400 Employee
    • Director of Translational Science
      • Sep 2020 - Aug 2023

      • Led the strategic planning and execution of translational studies to support early phase clinical trials exploring the potential of the macrophage targeting agent, eganelisib in combination with standard of care in metastatic triple negative breast cancer and metastatic urothelial carcinoma• Coordinated activities among networks of scientists, collaborators, external CROs and bioinformatic consultants to meet time-driven goals• Evaluated and prioritized preclinical and clinical collaborations to support the clinical development strategy as a member of the clinical-translational-preclinical (CTP) leadership team• Leveraged biomarker analysis to support the use of eganelisib in PD-L1 negative cancer • Proposed and executed company publication strategy as a member of the product leadership team• Generated and presented key scientific findings at medical conferences as an invited speaker and contributing author to poster presentations• Provided subject matter expertise for regulatory interactions and documents including protocols, investigator brochures, FDA briefing books and regulatory responses

    • Associate Director, Translational Science
      • Sep 2017 - Sep 2020

      • Operationalized Translational Medicine function for Phase 1 and Phase 2 clinical trials which included setting the strategy, developing a budget and contract oversight• Evaluated investigator sponsored trial (IST) proposals for fit within clinical development strategy• Collaborated with clinical pharmacology to evaluate pharmacokinetic-pharmacodynamic relationships (PK-PD studies)• Managed CROs, assuring data quality and assay optimization for Digital Spatial Profiling, RNAseq, Flow Cytometry, Luminex, Immunohistochemistry, Multiomyx• Managed a team of bioinformatics consultants developing a data analysis platform• Facilitated clinical operation activities for study start up including lab manual setup, site initiation visits training materials, protocol writing, and implementation of a sample tracking process

    • Lead Senior Scientist
      • Feb 2012 - Jul 2016
      • Cambridge, MA

      As a member of a highly integrated team of scientists, my primary responsibility was to support early discovery pipeline expansion efforts in oncology. I assisted in the evaluation of potential in-licensing opportunities as well as internal drug discovery programs by conducting relevant cell biology assays under strict timelines. As a lead senior scientist, I contributed to the initiation, execution, and evaluation of early discovery programs. I managed direct and indirect reports, led cross functional team meetings and presented my work in a variety of settings including conferences, team meetings and company wide program reviews.

    • Scientist
      • Jun 2011 - Feb 2012
      • Cambridge, MA

      As a scientist in the Therapeutic Discovery Group at Amgen, I worked in a highly collaborative, team-based environment to facilitate early stage target validation of small molecule programs in Oncology. I also performed assay development and cell line generation to support and enable early stage drug discovery efforts in Neuroscience and Oncology.

    • Post Doctoral Fellow
      • Mar 2005 - Jun 2011
      • Boston, MA

      As a post doctoral fellow in Wade Harper's lab, I utilized genomic and proteomic approaches to identify novel regulators of the DNA damage response. I performed a genome-wide RNAi screen for camptothecin sensitivity/resistance which led to the identification of a novel mammalian MMS22L-NKFBIL2 complex required for genomic stability.

  • Brown University
    • Providence, RI
    • Post Doctoral Research Associate
      • May 2004 - Mar 2005
      • Providence, RI

      As a post doctoral research associate in John Sedivy's lab, I studied the role of c-Myc in the regulation of transcription through promoter escape.

    • Chemistry Lab Technician VII, Cancer Research Group
      • May 1998 - Aug 1998

      Generated reagents and performed plate based assays to support early stage drug discovery efforts in Oncology.

    • Quality Control Laboratory Assistant VII, Technology Transfer Group
      • Dec 1996 - May 1998

      Trained and certified quality control laboratories in analytical methods at Pfizer branches including Groton, CT, Sandwich, England, and San Juan, Puerto Rico.

    • Quality Control Laboratory Assistant VI, Product Stability Group
      • Aug 1996 - Dec 1996

      Assayed drug potency and purity using high-performance liquid chromatography in compliance with good manufacturing practices (GMP).

Education

  • 1998 - 2004
    Brown University
    Doctor of Philosophy (PhD), Cell/Cellular and Molecular Biology
  • 1990 - 1994
    Brown University
    Bachelor of Science (BS), Biology

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Industry Focus. “Biotechnology and Pharmaceuticals”

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