Biologist | Biologe (m/w/d)

Job Summary

This role at a university hospital in Munich involves managing the quality assurance for clinical trials. You will act as the primary contact for clinical projects, addressing questions related to quality, regulatory affairs, and Good Clinical Practice (GCP). Key responsibilities include maintaining and developing quality management processes, SOPs, and the quality management handbook. You will also be responsible for creating audit plans, conducting audits, preparing for and supporting inspections, and managing corrective and preventive actions (CAPAs). Additionally, you will support study planning and execution by providing consultation and reviewing documents. The position requires a university degree in life sciences or a comparable qualification, knowledge of international regulations, and professional experience in quality management for clinical trials, ideally within the pharmaceutical industry or CROs. Strong IT skills and fluent German and very good English are essential.