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

akut... Kompetente Lösungen GmbH

Biberach an der Riß, Baden-Württemberg, Deutschland
Published Mar 26, 2026
Full-time
No information

Job Summary

As an IRT Expert for a global pharmaceutical player, you will lead the end-to-end lifecycle of study-specific Interactive Response Technology concepts. Your daily responsibilities include the independent planning, implementation, maintenance, and decommissioning of IRT systems within cross-functional project teams. You will act as a technical authority, ensuring that complex clinical study designs are translated into compliant systems that prioritize patient safety and drug security. A key part of the role involves validating computerized systems and ensuring all activities align with GMP, GCP, and international regulatory standards. This position is particularly attractive due to its hybrid work model (2-3 days remote), competitive salary package including performance bonuses, and the opportunity to work within a highly innovative pharmaceutical environment. The role offers a 37.5-hour work week and a clear path for professional development within a motivated team.

Required Skills

Education

Master's degree in Natural Sciences or a Bachelor's degree with extensive professional experience in a related scientific or quality-focused field.

Experience

  • Professional experience in IRT systems, including technical functions and implementation
  • Several years of experience in a scientific field or quality environment with a Master's degree, or extensive experience with a Bachelor's degree
  • Proven experience in the pharmaceutical industry regarding regulatory requirements
  • Experience in leading cross-functional project teams and managing complex study designs
  • Professional experience in the validation of computerized systems

Languages

German (Fluent)English (Fluent)

Additional

  • Hybrid work model requiring 2-3 days on-site; 18-month fixed-term contract with option for permanent hire; knowledge of international pharmaceutical guidelines (US/EU) required.