Biologist / Biotechnologist IRT Expert | Biologe (m/w/d) Biotechnologe (m/w/d) IRT Expert (m/w/d)
agento PersonalManagement GmbH
Job Summary
This role offers the opportunity to join a world-leading pharmaceutical company in Biberach, focusing on the development of life-improving medications. As an Interactive Response Technology (IRT) Expert, you will independently lead the assessment, planning, conceptual implementation, and maintenance of study-specific IRT concepts. You will serve as the primary IRT representative within cross-functional project teams, ensuring that technical implementations align with clinical trial designs, compliance standards, and drug safety protocols. The position involves contributing to the continuous evolution of IRT solutions and ensuring all activities adhere to GMP, GCP, and international regulatory guidelines. This is a hybrid role (2-3 days remote) that combines technical software lifecycle management with clinical trial operations. It is particularly attractive due to its competitive compensation (approx. €73,500 p.a.), high potential for permanent takeover, and the chance to work at a top-tier global employer dedicated to employee development.
Required Skills
Education
Master's degree in Natural Sciences (Biology, Biotechnology, or related) or a Bachelor's degree with extensive professional experience.
Experience
- Several years of professional experience in a related scientific field with a Master's degree, or extensive experience with a Bachelor's degree
- Proven expertise in the technical aspects and functions of IRT systems
- Professional experience in quality management and regulatory requirements within the pharmaceutical industry
- Experience with global investigational medicinal product activities and clinical study design
- Experience in the validation of computer-based systems and cloud-based software lifecycles
Languages
Additional
- This is a hybrid position requiring 2-3 days per week on-site in Biberach after the initial on-site training period. Candidates must be able to work within GMP/GCP and international regulatory frameworks (EU/USA).
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