Clinical Study Project Management: Take full responsibility for clinical trials in the role as sponsor and of non-interventional healthcare studies in fully outsourced model, steering scope, timelines and budget while safeguarding patient safety and data integrity. * Cross-functional Leadership & Compliance: Align research, quality, regulatory, legal and commercial stakeholders, consider interests and inputs from patients, investigators, and clinical experts, ensure compliance with all legal requirements, and resolve issues proactively to keep every project milestone on track. * Experience: Professional experience in clinical research project management (pharmaceutical industry or contract research organization) are an asset, but we are also open for structured and well-organized graduates. * Skills a
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