Line manager for the organization/project management of clinical studies in the Gastro II department * Preparation of cross-functional presentations for senior management (e.g., deep dives, global program updates, phase transitions) * Participation in reviewing the clinical sections of regulatory submission dossiers, documents for scientific consultations (e.g., Scientific Advice, PIP, benefit dossier, etc.), or orphan drug applications in consultation with the Head of Clinical Research * Participation in coordinating and drafting responses to clinical deficiency letters in regulatory procedures in consultation with the Head of Clinical Research * A minimum of 5 years of clinical development research and clinical study project management, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) at an international (Europe, USA, Australia) level is required
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