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for preclinical support of clinical program-related scientific objectives. This includes assessment of medical need, proposal of clinical development pathways, and re-view of preclinical data for clinical
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. This position reports to the Head Patient Safety Immunology. Key Responsibilities: • Providing expert safety input to the clinical development program for assigned projects/products, participating as an active
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Essential Requirements: * Ph.D or MD/Ph.D or equivalent training. * At least 3 years of postdoctoral experience in industry or equivalent. * Expertise in fibrosis biology, immunology/autoimmunity
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safety input to the clinical development program for assigned projects/products, participating as an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT
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Essential Requirements: * Ph.D or MD/Ph.D or equivalent training. * At least 3 years of postdoctoral experience in industry or equivalent. * Expertise in fibrosis biology, immunology/autoimmunity