Specialist, Clinical Trial Supply Management IRT Systems | Life Scientist (m/w/d)

Job Summary

This specialist role focuses on the critical area of Clinical Trial Supply Management (CTSM), specifically supporting Interactive Response Technology (IRT) systems for global Phase I-III clinical trials. Key responsibilities involve coordinating IRT system setup and ongoing maintenance, including meticulous User Requirement Specification (URS) reviews and participation in User Acceptance Testing (UAT). The specialist acts as a vital link, communicating study parameters to IRT vendors, managing budget workflows, and ensuring documentation integrity by maintaining the electronic Trial Master File (eTMF). The role requires providing basic IRT-related communication support and developing training materials for system users. Candidates must possess a Bachelor’s degree in a relevant field like Life Sciences or Computer Science and have a minimum of three years of professional experience in clinical trial supply or the pharmaceutical industry, coupled with business-level fluency in English. This position offers the opportunity to accelerate cutting-edge solutions from science to survival.