Manager of Clinical Drug Supply for Regeneron, overseeing Investigational Product requirements for clinical trials. Collaborating with various teams to ensure timely delivery and compliance with regulations.
Responsibilities
responsible for forecasting Investigational Product (IP) supply requirements for multiple clinical trials
managing the IP distribution process to one or more clinical trials
serves as lead drug supply manager for the functional area in supply planning
manages supply planning and timelines to ensure alignment with study plans
provides input to the development of IP-related study documents
manages and oversees investigational product (IP) inventory strategy
oversees IP shipment orders according to supply plans
works with cross-functional teams to develop specifications and support user testing of IRT systems
develops strategy and oversees drug return and destruction activities
coordinates with other functional areas to define ancillary and/or comparator supply strategy
compiles and reports supply status to study teams and senior management
leads management of IP service vendors
may mentor or coach junior Clinical Drug Supply & Logistics staff
Requirements
minimum of bachelor's degree
at least 6 years of relevant experience in the biotechnology/pharmaceutical industry
3 years minimum in clinical supply management
a Masters/MBA/PharmD with 3+ years of relevant industry experience is preferred
Benefits
health and wellness programs (including medical, dental, vision, life, and disability insurance)
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