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Accountable for the strategic leadership and operational excellence of global clinical trials, driving delivery across all phases and therapeutic areas. This role sets the vision for successful trial execution, influences organizational strategy, and
Provide epidemiology and statistical analytical support for RWE studies; Contribute to the development of evidence generation plans and design of RWE studies for scientific and regulatory purposes; Advise study teams on research methodologies and
Lead the development and execution of the Global Medical Affairs strategy for insomnia products; Serve as a core member of the Global Medical Affairs Leadership Team and Product Lifecycle Team; Manage and develop a small team of Global Medical Directors,
You will perform extractables/leachables (EL) and elemental impurities (EI) assessments according to Lonza procedures and best scientific practices; Act as Lonza’s global EL/EI subject matter expert (SME) and ensure regulatory compliance of the global
You will be responsible for developing and executing the global medical strategy and plan for the assigned product in collaboration with the rest of the global medical team, as well as supporting the necessary cross-functional workstreams, while adhering