Teresa Borowiecka

Clinical Study Manager in Phase I at Ryvu Therapeutics
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Contact Information
us****@****om
(386) 825-5501
Location
PL
Languages
  • English -
  • German -

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Experience

    • Poland
    • Biotechnology
    • 100 - 200 Employee
    • Clinical Study Manager in Phase I
      • Nov 2020 - Present

      Phase I study in solid tumor indications Phase I study in solid tumor indications

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Clinical Monitoring Project Lead
      • Feb 2015 - Oct 2020

      Outsourced to the Sponsor Janssen-Cilag to the hemato-oncology department. Main therapeutic area; Oncology; Renal cell carcinoma ( RCC), Brest Cancer Hemato-oncology; Multiple Myeloma (MMY), Chronic Lymphocytic Leukemia ( CLL), Indolent Non-Hodgkin Lymphoma ( iNHL), Mantle Cell Lymphoma ( MCL) Cardiology; Hypertension, Myocardial Infarction Vaccines; meningococcal, pneumococcal, influenza Gastrointestinal; Ulcerative Colitis Psychiatric; Major Depression More than 15-year commercial record (Pharma and CRO). Good practical knowledge and strong leadership skills

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • CMA (Clinical Monitoring Associate)
      • Jan 2014 - Dec 2014

      Responsibilities include: remote clinical monitoring tasks and remote visits of assigned projects in accordance with relevant SOPs, study specific procedures and regulations; managing, coordinating, and supporting clinical monitoring activities remotely, including issue resolution, patient enrollment management, sites’ payments, handling protocol, ICF and contract amendments, drug and supply management and ensuring timely data entry at a site level. Responsibilities include: remote clinical monitoring tasks and remote visits of assigned projects in accordance with relevant SOPs, study specific procedures and regulations; managing, coordinating, and supporting clinical monitoring activities remotely, including issue resolution, patient enrollment management, sites’ payments, handling protocol, ICF and contract amendments, drug and supply management and ensuring timely data entry at a site level.

    • Ireland
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Senior Clinical Research Associate
      • Oct 2007 - Dec 2013

    • United States
    • Research Services
    • 700 & Above Employee
    • Senior Clinical Research Associate
      • Aug 2005 - Sep 2007

    • Germany
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Clinical Research Associate
      • Jun 2003 - Jul 2005

Education

  • Jagiellonian University
    Master of Science (MSc), Environmental Science
    1996 - 2001

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