Teams at medac GmbH

Lead global clinical development programs (Phase I-III) for autoimmune/immunology assets. Design integrated development strategies (CDPs, TPPs), oversee multiple studies and data integrity, perform asset due diligence, manage lifecycle and indication/territory expansions, and lead regulatory interactions and submissions (EMA/FDA). Ensure high-quality clinical and regulatory documentation and drive cross-functional scientific leadership.

Support product lifecycle for a rheumatology portfolio: assist cross-functional teams (medical, commercial, regulatory), conduct market and competitor research, help plan launches and promotional activities, and track product performance and metrics.

Lead the SAP QM (inspect-to-release) stream in an S/4HANA implementation: design and transition end-to-end inspection and release processes, ensure master data quality, align with LIMS, coordinate internal/external teams, support gap analysis and change requests, prepare decision papers, and manage governance, reporting, risks, issues, and escalations.