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

BioNTech SE

Mainz am Rhein, Rheinland-Pfalz, Deutschland
Published Sep 19, 2025
Full-time
No information

Job Summary

As a Specialist, CTSM IRT Systems, you will be instrumental in managing Interactive Response Technology (IRT) systems for global Phase I-III clinical trials. Your daily tasks will involve collaborating with IRT vendors, coordinating system setup and maintenance, including User Requirement Specification (URS) reviews and User Acceptance Testing (UAT). You'll also assist in preparing UAT test scripts, participate in testing, and identify configuration risks. This role requires you to support budget management, develop user training materials, and maintain essential documentation within the eTMF. This position offers a unique opportunity to accelerate scientific breakthroughs by ensuring seamless delivery of cutting-edge solutions in clinical trial supply management.

Required Skills

Education

Bachelor’s degree in Computer Science, Information Systems, Life Sciences, Engineering, or a related discipline.

Experience

  • • Minimum 3 years of professional experience with exposure to clinical trial supply management or related areas in the pharmaceutical industry (preferred)

Languages

English (Fluent)

Additional

  • Not specified