Geoffrey M. Kuesters

Geoffrey M. Kuesters Email and Phone Number

Translation Medicine Leader @ Lifordi Immunotherapeutics, Inc.
Geoffrey M. Kuesters's Location
Greater Boston, United States, United States
Geoffrey M. Kuesters's Contact Details

Geoffrey M. Kuesters personal email

n/a
About Geoffrey M. Kuesters

Ph.D. scientist with industry experience in clinical development leading companion diagnostic, PK, ADA and biomarker plan development and execution for oncology and other indications. Additional skills include bioanalytical, clinical study activities, data management/programming/statistics CRO oversight, data analysis, assay development/validation, and management of multiple scientists. Self-motivated, detail-orientated scientist recognized for problem solving as well as scientific and operational contributions towards clinical and regulatory documents as well as internal, external and cross functional endeavors.

Geoffrey M. Kuesters's Current Company Details
Lifordi Immunotherapeutics, Inc.

Lifordi Immunotherapeutics, Inc.

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Translation Medicine Leader
Geoffrey M. Kuesters Work Experience Details
  • Lifordi Immunotherapeutics, Inc.
    Senior Director, Translational Medicine
    Lifordi Immunotherapeutics, Inc. Jan 2024 - Present
  • Celsius Therapeutics
    Senior Director, Biomarkers
    Celsius Therapeutics Jan 2023 - Present
    Cambridge, Massachusetts, Us
  • Rubius Therapeutics
    Director, Translational Medicine
    Rubius Therapeutics Jul 2019 - Nov 2022
    Cambridge, Massachusetts, Us
    Associate Director July 2019-Mar 2021Director Mar 2021-present
  • Merrimack Pharmaceuticals, Cambridge, Ma
    Head Of Companion Diagnostics And Biomarkers
    Merrimack Pharmaceuticals, Cambridge, Ma Jan 2016 - May 2019
    Director, Head of Companion Diagnostics and Biomarkers - Oct 2018 - presentAssociate Director, Head of Companion Diagnostics and Biomarkers - Jul 2017 - Oct 2018Principal Scientist - Jan 2017 - Jul 2017Senior Scientist - Jan 2016 - Jan 2017Scientist leading companion diagnostic and biomarker development supporting late pre-clinical, and Phase 1 and 2 clinical studies. Support clinical on multiple aspects of Phase 1 and 2 studies including data management, programming and statistics CRO oversight, patient enrollment, efficacy and safety review and vendor oversight. Lead development, validation and oversight of all programs’ pharmacokinetic and immunogenicity assays for GLP preclinical and clinical trial support. Significant collaboration across multiple functions including medical, clinical operations, pharmacovigilance, legal, research, quality and finance. Contribute companion diagnostic, biomarker, pharmacokinetic and immunogenicity for multiple publications, clinical study reports and regulatory documents. Experienced user of multiple data analysis and presentation tools including JMP, GraphPad Prism, Excel and Powerpoint.
  • Biogen
    Scientist I-Ii
    Biogen 2010 - 2015
    Cambridge, Ma, Us
    Lead scientist responsible for biomarker plan development, representing department on various cross-functional teams, contributing to clinical protocol development and regulatory submissions/responses, and development. This included qualification/validation, transfer and oversight of multiple matrix pharmacokinetic, immunogenicity and biomarker assays for clinical trial and commercial support as well as associate scientist management.
  • Northeastern University
    Ph.D. Graduate
    Northeastern University 2006 - 2010
    Boston, Ma, Us
    Graduated from Northeastern University with a PhD in Pharmaceutical Sciences and Drug Delivery Systems. Ph.D. Thesis: Development and Evaluation of Bevacizumab-Modified Pegylated Cationic Liposomes Using Cellular and In Vivo Models of Human Pancreatic Cancer
  • Biogen Idec
    Associate Scientist I-Ii
    Biogen Idec 2003 - 2006
    Cambridge, Ma, Us
    Responsible for developing, executing, and troubleshooting both manual and automated assays, including cell adhesion, cell bridging, lysate inhibition, and Kinase Receptor Activation (KIRA) potency or product characterization assays.
  • Consensus Pharmaceuticals
    Research Associate
    Consensus Pharmaceuticals 2001 - 2003
    Responsible for evaluating, developing, and executing enzyme (protease/kinase) kinetic, GPCR inhibition, cytoxicity, calcium flux and ELISA assays utilized by the Assay Group.
  • Millennium Pharmaceuticals, Inc.
    Intern
    Millennium Pharmaceuticals, Inc. 2000 - 2000

Geoffrey M. Kuesters Skills

Elisa Assay Development Biotechnology Drug Delivery Drug Discovery Cell Culture Life Sciences Pharmacokinetics Glp Biomarker Discovery Biomarker Development Immunogenicity People Management Assay Validation Drug Development Hplc Protein Chemistry Clinical Study Design Teamwork Cell Based Assays Regulatory Filings Enzyme Kinetics Cro Western Blotting Good Laboratory Practice Cro Management Clinical Protocols Product Characterization Potency Assays Liposomes Medical Affairs

Geoffrey M. Kuesters Education Details

  • Northeastern University
    Northeastern University
    Pharmaceutical Sciences And Drug Delivery Systems
  • Boston College
    Boston College
    Biology

Frequently Asked Questions about Geoffrey M. Kuesters

What company does Geoffrey M. Kuesters work for?

Geoffrey M. Kuesters works for Lifordi Immunotherapeutics, Inc.

What is Geoffrey M. Kuesters's role at the current company?

Geoffrey M. Kuesters's current role is Translation Medicine Leader.

What is Geoffrey M. Kuesters's email address?

Geoffrey M. Kuesters's email address is ge****@****stx.com

What schools did Geoffrey M. Kuesters attend?

Geoffrey M. Kuesters attended Northeastern University, Boston College.

What skills is Geoffrey M. Kuesters known for?

Geoffrey M. Kuesters has skills like Elisa, Assay Development, Biotechnology, Drug Delivery, Drug Discovery, Cell Culture, Life Sciences, Pharmacokinetics, Glp, Biomarker Discovery, Biomarker Development, Immunogenicity.

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