Responsibilities include:

•  Coordinate labeling, packaging, and shipment of packed supplies.
• Create and provide multiple planning scenarios based on various combinations of inputs and variables, as required.
• Lead forecasting meetings with key stakeholder to ensure the adequacy of supply/re-supply and
• Assess issues with regards to study design, supply availability, and timelines.
• Promptly identify and escalate risks to study supply to all key stakeholders and internal management.
• Represent GCSCM in cross-functional teams and projects at the direction of GCSCM management.
• Strategize with study managers and review study protocols to determine appropriate packaging configurations, blinding techniques, and optimal distribution plans.
• Actively participate in planning meetings to ensure that project needs, priorities, and timing are understood. 
• Serve as the primary interface with Clinical Development, Quality, Biostatistics, Regulatory Affairs, Corporate Planning, and Operations to ensure coordination of all activities necessary to fulfill the supply plan.
• Provide input to matrix teams on timing, resourcing, and budget projections
• Determine distribution strategies for global studies.
• Articulate clinical supply chain management processes and strategies to key stakeholders.
• Review and update existing procedures and SOPs; identify the need for and assist in the establishment of new procedures and SOPs.