Project Leader/Manager responsible for end - to - end project contributions at a technology company. Managing documentation, deployments, and collaborating across technical and functional teams.
About the role
- 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)
- fitness centers
- 401(k) company match
- family support benefits
- equity awards
- annual bonuses
- paid time off
- paid leaves (e.g., military and parental leave)
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