Veronica Ventura

Technical Project Manager at Corat Therapeutics GmbH
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Contact Information
us****@****om
(386) 825-5501
Location
Brunswick, Lower Saxony, Germany, DE
Languages
  • Catalan Native or bilingual proficiency
  • Spanish Native or bilingual proficiency
  • English Full professional proficiency
  • French Elementary proficiency
  • German Professional working proficiency

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Credentials

  • Diploma in Project Management
    Alison - Empower Yourself
    Nov, 2021
    - Nov, 2024

Experience

    • Germany
    • Biotechnology Research
    • 1 - 100 Employee
    • Technical Project Manager
      • Dec 2021 - Present

    • United States
    • Research
    • 300 - 400 Employee
    • Senior Scientist & Study Director
      • Sep 2015 - Sep 2019

      Senior Scientist responsible for the overall implementation of the qPCR laboratory and the qPCR studies carried out in the Bioanalytical Department: gene expression analysis, biodistribution of gene therapy products. Senior Scientist responsible for the overall implementation of the qPCR laboratory and the qPCR studies carried out in the Bioanalytical Department: gene expression analysis, biodistribution of gene therapy products.

    • Biotechnology Research
    • 100 - 200 Employee
    • Study Director. Bioanalytics, Metabolism and Screening Department.
      • Feb 2012 - Sep 2015

      Study director of bioanalytical and drug metabolism studies. Apart from previous background in drug metabolism studies, adquiring experience in all kind of studies related to bioanalytics (bioanalysis in plasma/serum or tissues, determination of biomarkers) and dose formulation analysis. Including validations and sample analysis following GLP and the current bioanalytical guidances. Analysis by UPLC-MS/MS, HPLC- UV, Fluorescence or Radiochemical detection, qPCR and ELISA Study director of bioanalytical and drug metabolism studies. Apart from previous background in drug metabolism studies, adquiring experience in all kind of studies related to bioanalytics (bioanalysis in plasma/serum or tissues, determination of biomarkers) and dose formulation analysis. Including validations and sample analysis following GLP and the current bioanalytical guidances. Analysis by UPLC-MS/MS, HPLC- UV, Fluorescence or Radiochemical detection, qPCR and ELISA

    • France
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Drug Metabolism Scientist
      • Sep 2004 - Dec 2011

      Study director of drug metabolism studies in accordance with the Good Laboratory Practices (GLP). 7 years experience in studies related to drug metabolism and disposition: in vitro metabolite profiling and interspecies comparison, in vitro CYP inhibition, CYP induction (including determination of mRNA expression by qPCR), phenotyping, metabolite identification, plasma protein binding studies, and in vivo metabolite profiling (from ADME and clinical studies). Coordination of studies with CROs. Development, optimization and validation of new assays. Experimental skills on in vitro assays and cell cultures. Analysis of samples by HPLC, LC-MS, radiochemical detection, Real Time PCR. Show less

    • Pharmacist
      • Jun 2003 - Aug 2004

    • Pharmacist
      • Feb 2001 - May 2003

Education

  • Universitat de Barcelona
    PhD, Biotechnology
    2008 - 2013
  • Universitat de Barcelona
    Master in Molecular Biotechnology
    2006 - 2008
  • Universitat de Barcelona
    Master in Experimental Pharmaceutical Sciences, Biochemistry and Molecular Biotechnology
    2003 - 2004
  • Universitat de Barcelona
    Pharmacy
    1998 - 2003

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