Job Summary

The Sen. CSCM is responsible for planning and managing designated Clinical Supply Chain Management activities for the Fisher Clinical Services (FCS) Clinical Supply Optimization Services (CSOS) unit. This position will work with FCS clients, packaging sites, depots, Clinical Supply Chain Managers and Drug Supply Coordinators to understand the supply chain requirements define the supply strategy and manage clinical trial materials on the study or program level. They will also participate & support the commercial team as Subject Matter Expert for business development activitieResponsibilities:

  • Serves as a subject matter expert on the Clinical Supply Chain Optimization Services (CSOS) service line and is instrumental in leading team efforts in support of positioning the service offering in the market place.
  • Interprets protocols to build compound and/or study level plans that enable planned enrollment and are adaptable to the changing requirements of a study including securing Clinical Supply Chain Management (CSCM) support and delegating study tasks to team members as appropriate.
  • Leverages drug supply related capabilities of the IRT to appropriately manage studies responsible for the management of designated trials actively performing CSCM responsibilities including project management, Quoting & Invoicing, forecasting, simulation, IRT, development of labeling strategies, packaging plans, drug product requirements planning, distribution network planning, time management, temperature excursion management and planning for study drug returns and reconciliation.
  • Conducts regular team meetings to assess the status of studies, identifies necessary resources, and proactively addresses issues.
  • Key account responsibility
  • Maintains appropriate metrics to ensure business success
  • Responsible for budgetary aspects including personnel expenses, and other related costs
  • Works closely with the CSOS leadership to ensure best practices, training and procedural aspects are aligned globally
  • Works with other team leaders to ensure global processes and procedures are developed and followed and there is consistency between programs.
  • Works with Fisher Clinical Services Clients, CSCM’s, Program Managers and the FCS sales force to understand the supply chain requirements to support Clinical Trials.
  • Demonstrates the ability to promote the company vision
  • Utilizes an extensive network in the pharmaceutical industry to generate and cultivate leads for the growth of the businesses
  • Represents and appropriately positions the services for potential clients
  • Utilizes understanding of Clinical Trial Supply Chain Management best practice principles to develop new or improve existing business processes and appropriately document and revise or develop associated training materials
  • Guidance / Coaching and Support for the Simulation team incl. run own Simulation studies incl. advice and output presentation to sponsors
  • Stays abreast of relevant GxP and other regulatory requirements and ensures study management activities are aligned
  • Attends relevant client related meetings and appropriately represent status of the Clinical Supply Chain
  • Conducts activities in a safe and efficient manner
  • Manage own clinical trials / protocols
  • Other duties may be assigned to meet the needs of the business



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