Lead operational execution of clinical trials Manage CROs, study vendors, and investigative sites Oversee timelines, budgets, and milestone tracking Coordinate cross-functional teams (clinical, regulatory, safety, data) Support site initiation, patient enrollment acceleration, and monitoring oversight Proactively identify and mitigate operational risks Report project status to senior management

Bachelor’s degree or higher in life sciences or related field Minimum 6 years of experience in clinical project management (biotech or CRO) Experience managing multi-center clinical trials Willingness to travel frequently Strong knowledge of ICH-GCP guidelines Excellent organizational and communication skills Fluent in English

Lead clinical development strategy for the autoimmune program Author and oversee clinical trial protocols Contribute to global regulatory interactions (FDA, EMA, Swissmedic) Design and supervise patient screening and enrollment strategies Collaborate with CROs, investigators, and KOLs Interpret clinical data and support external communications (partners, investors) Contribute to lifecycle and indication expansion strategy

MD (preferred) or advanced degree in clinical medicine Minimum 7 years of clinical development experience in biotech/pharma Experience in immunology, dermatology, or inflammatory diseases preferred Strong understanding of IND-to-PoC development pathway Proven experience in protocol writing and clinical study documentation Fluent in English