Analyse clinical trial protocols and translate requirements to establish an efficient supply chain solution for PSI studies * 3-5 years experience in Clinical Supply Chain Management (Essential) * Experience working with supply chain technologies (i.e. IRT, CTMS, IWRS integration rules and principles) In this role, you will undertake activities to assess, plan and set up trial supply schemes for assigned projects and manage vendors involved in clinical supplies and interactive response technology. * Plan the optimal campaign strategy, to ensure clinical supplies are available in accordance with the project requirements * Manage the vendor - oversee packaging, labelling, procurement, distribution and QP release activities to ensure supplies are delivered on time * Develop clinical supply plans and provide input for the development of management plans
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