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Own EU regulatory strategy for assigned programs from First-in-Human through pivotal development and marketing authorization; Serve as primary EU regulatory contact for cross-functional teams and provide clear, actionable regulatory guidance while
Lead the design and execution of clinical pharmacology strategies and corresponding studies across multiple programs. Develop innovative and meaningful clinical pharmacology approaches that accelerate and de-risk drug development Define dose selection,
Act as the Safety Science representative in the Medical Development Team (MDT) and ensure integration of safety into product development and lifecycle decisions; Provide clinical safety input into study design, conduct, analysis and interpretation,
Responsible for providing lead medical input and expertise to clinical development programs conducted for Therapeutic Dermatology products. Acting on the responsibility, the Head of Medical Experts, Therapeutic Dermatology, secures that clinical
Lead the nonclinical toxicology strategy across multiple research and development programs, ensuring alignment with program objectives and timelines as well as regulatory expectations; Provide scientific leadership for the design