Specialist, Clinical Trial Supply Management (CTSM) IRT Systems | Informatiker (m/w/d)

Job Summary

This specialist role focuses on the critical setup and ongoing maintenance of Interactive Response Technology (IRT) systems globally, supporting innovative Phase I-III clinical trials. The successful candidate will act as a key collaborator, communicating study parameters to IRT vendors under the guidance of the IRT Manager. Day-to-day responsibilities involve coordinating system setup, conducting User Requirement Specification (URS) reviews, and executing User Acceptance Testing (UAT), including preparing test scripts and identifying configuration risks. Furthermore, the role involves managing budget and category-invoice workflows, supporting user training by developing essential materials, and ensuring documentation integrity by uploading materials to the electronic Trial Master File (eTMF). This position requires a proactive individual with a Bachelor’s degree in Computer Science, Life Sciences, or a related field, and foundational professional experience in clinical trial supply management within the pharmaceutical industry.