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ZEG Berlin GmbH

Zentrum für Epidemiologie und Gesundheitsforschung

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Mohammed Dagher

Project Manager

Mohammed Dagher

Mohammed Dagher leads projects in the field of Real-World Evidence (RWE), epidemiological and clinical trials. In the RWE, he is responsible for designing and implementing secondary data-driven non-interventional studies. His duties include developing medical algorithms and interpreting big medical data sets for secondary data projects. These projects cover diverse topics such as Epidemiology, HEOR, Safety, and a broad range of therapy areas. In the epidemiological studies, he manages different non-interventional, observational studies in various therapeutic areas according to international standards.

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. Besides his pharmacy degree, he has a dual master’s degree in public health and European public health with a focus on pharmacoepidemiology from Hamburg University of Applied Sciences, Germany.

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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
  • Ulrike Amann-Gassner
  • Armin Papkalla
  • Silke Zimmermann
  • Nik Kolb

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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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