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ZEG Berlin GmbH

Zentrum für Epidemiologie und Gesundheitsforschung

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Elisabeth Finger

Director of Quality Management

Elisabeth Finger develops and manages the organizational-wide quality system, including strategic plans and policies, processes and procedures in compliance with applicable internal and regulatory requirements and guidelines. As part of this, she leads the interdepartmental quality management team which has its focus on the implementation and sustainment of a continuous improvement culture. She undertakes regular subcontractor audits during study conduct and internal quality audits to insure effective operations and compliance. Elisabeth is responsible for the corrective and preventive action management as part of the continuous quality improvement process. In an additional role, Elisabeth works as Study Data Manager to keep the practical scope as part of the Study Team in ZEG Berlin’s studies.

Elisabeth obtained her degree as Diplom-Dokumentarin (FH) in Medical Documentation at the University of Applied Sciences Hanover in 2008. She worked several years as Clinical Research Associate and Clinical Data Manager as basis for the different aspects of quality management before starting work at ZEG in 2014. In addition, Elisabeth took part in various further vocational trainings regarding Study Data and Quality Management.

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Executive Team

  • Clare Barnett
  • Karl Pauls
  • Michael Schultze
  • Alfred Pauls
  • Anja Bauerfeind
  • Do Minh Thai
  • Elisabeth Finger
  • Jens A. Lange

Management Board

  • Klaas Heinemann
  • Clare Barnett
  • Marc Pignot
  • Karl Pauls
  • Johanna Poppe

Project Management Team

  • Pauline De Corte
  • Lisa Eggebrecht
  • Maria Cabral
  • Anitha Pitchika
  • Mohammed Dagher

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ZEG Berlin

Berlin Center for Epidemiology and Health Research

Invalidenstraße 115
10115 Berlin
Germany

Contact Us

Expertise

  • Real-World Evidence
  • Non-interventional study design
  • Post-authorization safety studies
  • Post-authorization efficacy studies
  • Cohort studies
  • Case-control studies
  • Medical Devices
  • Diagnostic tools
  • Data collection instruments

Services

  • Crisis Management
  • Consulting
  • Data Management and Biostatistics
  • Medical Writing
  • Study Management
  • Quality Assurance
  • Pharmacovigilance

ENCePP

We are a partner centre of the ENCePP scientific network which is coordinated by the European Medicines Agency. We are dedicated to excellence in research by adhering to the ENCePP Guide on Methodological Standards and promoting scientific independence and transparency. We register studies in the ENCePP E-Register of Studies, a publicly accessible resource for the registration of pharmacoepidemiological and pharmacovigilance studies.

General Data Protection Regulation

With a view to the introduction of the GDPR/EUDSGVO we are glad to present our newupdated privacy policy . The updated description are stored under “about us” and then “privacy policy/GDPR”. Further translation for study participants will follow contemporary.

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