Interactive Response Technology (IRT) Expert | IRT Expert (m/w/d)

Job Summary

As an IRT Expert, you will take ownership of the full lifecycle of study-specific IRT concepts, including planning, implementation, maintenance, and decommissioning. You will serve as the primary IRT representative within cross-functional clinical study teams, ensuring that technical implementations align with complex study designs, patient safety protocols, and international regulatory standards such as GMP and GCP. A key part of your role involves contributing to the continuous improvement of IRT systems to maintain state-of-the-art functionality and supporting the validation of computerized systems. This position is ideal for a professional with a background in clinical research or pharmaceutical sciences who thrives in a collaborative, innovative environment. You will benefit from a hybrid working model, professional development opportunities, and the chance to work with a global player in the pharmaceutical industry, ensuring that clinical trial logistics are executed with precision and compliance.