Associate Director Clinical Program Management - 12 months à Lucerne

Associate Director Clinical Program Management - 12 months Lucerne

À propos de notre clientOur client is a global pharmaceutical corporation with its regional headquarter based in Switzerland.Description du poste* Accountable for delivery of assigned clinical studies in compliance with procedural documents, SOPs, Code of Federal Regulations, Good Clinical Practices, ICH Guidelines, and all applicable regulations within the Clinical Development Plan (CDP) and according to the VBU operating model. * Responsible for the roll-out and maintenance in assigned clinical studies of risk-management approach defined for program. * In alignment with the applicable operating model, lead the cross functional SET in close collaboration with the CRO, providing oversight to ensure study goals and KPIs are met, with expected quality on schedule and on budget. * Contribute to protocol and/or synopsis, as well as the Clinical Study Report development. * Lead the ...

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