To strengthen our team we are looking for a 

Medical Data Reviewer/Clinical Trial Scientist (f/m/d), full-time

Germany, homeoffice

Ref.-Nr. S-1035

Your Tasks
professional support in conducting international clinical trials:
• preparing medical data review plans
• safety reviews
• developing study-specific tables and listings
• writing study specific safety reports, summaries and status reports

support in developing Clinical Data Management tools and processes:
• exploring technical possibilities in automation of Data Management processes
• improving standardization of processes in Data Management
• providing contributions to accelerate Data Management routines
• working in a multidisciplinary, international team

Your Profile
• university degree in natural sciences (biology, chemistry, pharmacy etc.) / life sciences
• clinical or scientific experience in oncology strongly preferred
• experience in clinical research (e.g. as CRA, Clinical Monitor, Clinical Trial Assistant, CTA, Clinical Data Manager) or in drug safety (pharmacovigilance) strongly preferred
• experienced in Clinical Data Management / Databases
• experienced in EDC-systems like RAVE
• experienced in Data visualization Tools like Tableau or Spotfire
• good knowledge of MS-Office with advanced MS-Excel skills
• good knowledge of medical review tools
• interested in a position in an innovative and highly structured environment
• strong organizational and team-working skills
• fluent in English (both written and spoken)

Your Chance
• outstanding qualification opportunities in the field of global clinical research
• permanent contract
• attractive salary
• long-lasting perspective in the pharmaceutical industry
• homeoffice
• company laptop and mobile phone

Your Initiative
If you are interested in this position and your profile fits to our requirements, we look forward to receiving your detailed application including CV and references via email (all documents as pdf-files only) to


Svelte scientific GmbH • Friedrichstraße 171 • 10117 Berlin •

Weiterleiten Drucken Zurück zur Übersicht