Job Description: This individual contributor is responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines Adopt supply strategies in view of changes in trial execution and ensure a seamless transition from study design phase Assess clinical study recruitment rates and ensure supply planning is adopted accordingly Utilize business tools to manage inventories at depots and sites and ensure on-time delivery with minimal overage of clinical supplies Conduct issue resolution activities for supply aspects of clinical studies (e.g., packaging, distribution) Establish and modify trial specific distribution agreements
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