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Trial Supply Manager
Ref No.: 18-20299
Location: TITUSVILLE, New Jersey
Trial Supply Manager
Titusville, NJ
1+ Year Contract 

This individual contributor is responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines.
Description of the Role: 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
Member of appropriate GCO clinical trial team.
Develop strong internal collaboration with GCO stakeholders to ensure customer satisfaction.
Interface with Global Trial Managers.
Manage trial supply budget.
Develop excellent working relationships with the other groups within Supply Management.

Responsible for the management of all clinical supplies during trial execution within company Pharma RnD (large and small molecules and for all phases of clinical trials).

Critical Experiences Required: A university/bachelor's degree (or equivalent experience) and 4-6 years' experience preferably in a clinical supply related role
Experience with clinical supply demand management tools preferred (e.g., tcVisualize, IVRS, SAP)
Experience with the following functions preferred: clinical supply pack/label/distribution, clinical trial operations, project management, pharma/bio research and development, inventory management
General knowledge of GxP principles
Intermediate to advanced software skills (e.g., Microsoft Excel, Powerpoint)