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ZEG Berlin GmbH

Zentrum für Epidemiologie und Gesundheitsforschung

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Director of Study Data Management (m/w/d)

Posted: 2025-03-20

The Center for Epidemiology and Health Research Berlin GmbH (ZEG Berlin) is an independent research institute with more than 50 colleagues from over 20 different nationalities in the heart of Berlin, whose focus is on the planning, implementation, and evaluation of large, international observational and long-term studies – and has been for over 30 years.
In 2023, Oracle became the majority shareholder, opening a new perspective for ZEG Berlin to operate within an internationally renowned large corporation. Despite all this, we have been able to maintain our family, social, and open corporate culture, which means that we always put people first.

We are looking for a full-time Director of Study Data Management who oversees the data management tasks and supervises all technical aspects concerning study data management.

 

What you can expect:

  • You coordinate internal resources and external contractors for the execution of data management procedures within ZEG Berlin projects
  • You have mainly administrative and personnel tasks, i.e., no (or less) operational
  • You support the Managing Director in preparing requests for study proposals
  • You ensure resource availability and allocation within the data management team
  • You measure project performance using appropriate tools and techniques
  • You contribute to the development of study-specific working procedures and data management SOPs and guidelines
  • You coordinate the tasks between the data management team members and advise them of their duties
  • You conduct regular personal interviews and job interviews with staff members, as required

 What we are looking for:

  • Academic degree or certificate(s) of achievement demonstrating relevant expertise in medical informatics, information science, computer science, or related areas
  • Ideally, 5 or more years of experience in data management
  • Significant experience in clinical or epidemiological data management, experience in (pharmaco-)epidemiological data preferred
  • Experience in leading a team, including excellent supervisory and organizational skills
  • Experience in electronic data capture (EDC) and other database systems is desirable
  • Understanding of Statistical Administration Software (SAS) and SQL/MySQL
  • Understanding of the Clinical Data Interchange Standards Consortium (CDISC) is preferred
  • Fluent in English and conversational German (B1)
  • Excellent problem-solving and analytical skills

What do we offer:

  • Familiar, social, and open company culture with 50+ colleagues
  • An open, motivating, and international working atmosphere
  • We organize regular company events where you will get to know your colleagues
  • Challenging tasks with variety and plenty of scope for team interaction in an appreciative working environment
  • Permanent employment contract
  • Flexible working time accounts for a good work-life balance
  • Company pension scheme
  • A full-time position with 30 days’ holiday and appropriate pay
  • Flat hierarchies, short decision-making processes, and family-friendly conditions
  • Home office possibility
  • Individual and professional development opportunities
  • Attractive location with excellent public transport connections

 

Are you interested?
Then, we look forward to receiving your meaningful application!

As Oracle Recruiting carries out the recruitment process on behalf of ZEG Berlin, please apply via the following link: https://eeho.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/jobsearch/job/269939.

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ZEG Berlin

Berlin Center for Epidemiology and Health Research

Invalidenstraße 115
10115 Berlin
Germany

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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.

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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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