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ZEG Berlin GmbH

Zentrum für Epidemiologie und Gesundheitsforschung

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    • Real-World Evidence
    • Non-interventional study design
    • Post-authorization safety studies
    • Post-authorization efficacy studies
    • Cohort studies
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    • Menopause Rating Scale
      • Menopause Rating Scale (MRS) – Languages
    • Aging Male Symptoms Scale
      • AMS – properties as an outcome measure
      • AMS – properties as a screening tool
    • Quality of Sexual Function Scale
      • Quality of Sexual Function Scale
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      • Short Term Hormone Effect Scale
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Project Management Team

Pauline De Corte

Project Manager

Pauline De Corte, project manager, is an integral member of the project management team, working as lead Project Manager for several ZEG Berlin studies.Read More

Lisa Eggebrecht

Project Manager

Lisa Eggebrecht is part of the project management team at ZEG Berlin and has successfully managed several non-interventional, observational studies in various therapeutic areas.Read More
Mohammed Dagher

Mohammed Dagher

Project Manager

Mohammed Dagher is a project manager in the field of Real-World Evidence (RWE). His interdisciplinary experience comprises medical/pharmaceutical expertise and advanced project management skills. In addition, he is a practitioner clinical pharmacist and an experienced pharmacovigilance manager in the clinical trial setting.Read More

Armin Papkalla

Project Manager

Armin has over 20 years of experience in clinical trials across various indications and phases, including NIS. He has worked as a Clinical Research Associate in oncology and transplantation, spent 12 years at the Hannover Clinical Trial Center GmbH, and served as a senior project manager at the Hannover Medical School. He holds a doctorate in Virology and a diploma in Biology from the University of Erlangen-Nürnberg, Germany.Read More

Silke Zimmermann

Project Manager

Silke Zimmermann is a project manager with extensive experience in managing and monitoring academic and industry-sponsored clinical trials, including pharmaceutical, medical device, and observational studies. She holds a doctorate in Natural Sciences from Leibniz University Hannover and has strong expertise in project and quality management. Since 2023, she has been a member of ZEG Berlin.Read More

Nik Kolb

Project Manager

Nik is a Senior Project Manager at ZEG Berlin, specializing in real-world evidence studies using secondary data and pharmacoepidemiology. He brings extensive experience from leading EMA-mandated PASS projects at a large global CRO.Read More

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Executive Team

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

Management Board

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

Project Management Team

  • Pauline De Corte
  • Lisa Eggebrecht
  • Mohammed Dagher
  • Armin Papkalla
  • Silke Zimmermann
  • Nik Kolb

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Expertise

  • Non-interventional study design
  • Post-authorization safety studies
  • Post-authorization efficacy studies
  • Cohort studies
  • Case-control studies
  • Medical Devices
  • Patient Reported Outcomes (PROs)
    • Aging Male Symptoms Scale
    • Menopause Rating Scale
    • Scale for Quality of Sexual Function
    • Short Term Hormone Effect Scale
    • Research team
  • Data collection instruments

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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
  • Patient Reported Outcomes (PROs)
  • 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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