Claudia Ose

Professorin für Medizinisches Informationsmanagement, Fliedner Fachhochschule Düsseldorf at Fliedner Fachhochschule Düsseldorf
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Contact Information
us****@****om
(386) 825-5501
Location
Essen, North Rhine-Westphalia, Germany, DE
Languages
  • Deutsch Native or bilingual proficiency
  • Englisch Professional working proficiency
  • Französisch Elementary proficiency
  • Arabisch Elementary proficiency
Skills

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Credentials

  • Introduction to Data Curation for SAS Data Scientists
    SAS
    Apr, 2020
    - Oct, 2024

Experience

  • Fliedner Fachhochschule Düsseldorf
    • Germany
    • Higher Education
    • 1 - 100 Employee
    • Professorin für Medizinisches Informationsmanagement, Fliedner Fachhochschule Düsseldorf
      • Aug 2018 - Present

  • University Hospital Essen
    • Germany
    • Hospitals and Health Care
    • 100 - 200 Employee
    • Senior Advisor Clinical trials
      • Aug 2019 - Present

  • Center for Clinical trials, University Hospital Essen
    • Essen
    • Managing Director
      • Apr 2006 - Jul 2019

      Establishment of the Center of clinical trials in the university and the German network of clinical trials Design and management of clinical trials in several indications (e.g. psychiatry, neurology, nephrology, oncology. pediatrics, surgery). Statistical analysis of these trials and report writing according ICH-E3. Team leadership for relevant clinical trials Updating SOPs Setup investigator training in the university. Lectures for investigators and trial assistants Cost accounting, acquisition of third-party funds and keeping in contact with clients Show less

  • Institute for Medical Informatics, Biometry and Epidemiology, University Hospital of Essen,
    • Essen
    • Project manager
      • Sep 1994 - Apr 2006

      Design, management and monitoring of clinical trials in several indications (e.g. Angiology, phlebology, epidemiology and public health, oncology, non-conventional therapies, hepatology, psychiatry, neurology, pediatrics, surgery). Statistical analysis of these trials and report writing according ICH-E3. Development of 22 Standard Operation Procedures (SOP) Design of a standardized trial protocol fitting for all clinical trial according GCP (Ose, 2001) Lectures in monitoring and in GCP at university and invited lectures for the GMDS Reviewing of publications and trial protocols Cost accounting, acquisition of third-party funds and keeping in contact with clients Show less

  • Freelancer
    • SAS-programmer, biometrician
      • Jul 1990 - Aug 1994

      Statistical analyses of clinical trials with SAS Writing of statistical reports Design of clinical and epidemiological trials and client counseling Statistical analyses of clinical trials with SAS Writing of statistical reports Design of clinical and epidemiological trials and client counseling

Education

  • Universität Duisburg-Essen
    Dr. rer. medic.
    2015 - 2018
  • Universität Duisburg Essen
    Master of Science (M.Sc.), Master of pharmaceutical Medicine
    2013 - 2015
  • University Hospital of Ulm for Medical documentation
    medical information management, 1,5
    1986 - 1989

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