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

agento PersonalManagement GmbH

Biberach an der Riß, Baden-Württemberg, Deutschland
Published Mar 20, 2026
Full-time
Permanent

Job Summary

This role involves leading the end-to-end lifecycle of study-specific Interactive Response Technology (IRT) concepts within a top-tier pharmaceutical environment. As an IRT Expert, you will independently manage the assessment, planning, conceptual implementation, maintenance, and decommissioning of these systems. You will serve as the primary IRT representative in cross-functional project teams, ensuring that technical implementations of clinical study designs align with drug safety and compliance standards. The position is highly collaborative, requiring you to contribute innovative solutions to keep systems at the cutting edge of technology while ensuring all activities adhere to GMP, GCP, and international regulatory guidelines. This is a hybrid role based in Biberach, offering a meaningful opportunity to contribute to the development of life-improving medicines within a company known for high employee satisfaction and professional growth.

Required Skills

Education

Master's degree in Natural Sciences (Biology, Biotechnology, or related) or a Bachelor's degree with extensive professional experience in a related field.

Experience

  • Professional experience in the IRT field with deep technical knowledge of system functions
  • Several years of experience in a scientific field for Master's degree holders or extensive experience for Bachelor's degree holders
  • Proven experience in quality management and regulatory compliance within the pharmaceutical industry
  • Experience in the validation of computerized systems and global clinical trial operations
  • Professional experience in cross-functional project leadership

Languages

English (Fluent)

Additional

  • Hybrid work model (2-3 days remote/home office); Initial training conducted on-site in Biberach; Knowledge of US, EU, and international pharmaceutical guidelines required.