Project Coordinator, Clinical Supply

About the Role

• Serves as an individual contributor responsible for project management of key Clinical Supply Chain documentation, tasks, and simple packaging activities in a GMP environment.

Key Responsibilities

• Planning, scheduling, coordination, and execution in support of CSPMs to ensure the timely availability of investigational drug supplies and related services to clinical sites and depots.
• Translates stability and packaging requests into an executed packaging design.
• Identifies, develops, communicates, and tracks task completion dates, activities, logistics, and milestones in support of CSPMs to ensure the timely availability of investigational drug supplies.
• Creates appropriate protocol-specific manufacturing and packaging work orders in concert with the CSPM.
• Completes, upon request of the CSPM, tasks identified for the Center of Excellence team.

Key Stakeholders

• The Clinical Drug Supply Chain including R43E, Analytical, Quality, and globally with Germany counterparts for the transfer of clinical drug from Lake County.

Qualifications

• Education: Bachelor’s Degree required, preferably in physical science, math, engineering, or pharmacy.
• 0 - 2+ years total experience in the Pharmaceutical Industry.