Project Coordinator, Clinical Supply
AbbVie
North Chicago, IL0–2 yrs1d agovia LinkedIn
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 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 to ensure the timely availability of investigational drug supplies.
- Creates appropriate protocol-specific manufacturing and packaging work orders.
- Completes tasks identified for the Center of Excellence team, upon request.
Key Stakeholders
- The Clinical Drug Supply Chain including R43E, Analytical, Quality, and globally with Germany counterparts.
Requirements & Tech Stack
- GMP environment
- Clinical Supply Chain documentation
- Packaging activities
- Clinical sites and depots
- Stability and packaging requests
- Packaging design
- Task completion dates
- Logistics
- Milestones
- Manufacturing and packaging work orders
- Center of Excellence team
Qualifications
- Education: Bachelor’s Degree required, preferably in physical science, math, engineering, or pharmacy.
- 0 - 2+ years total experience in the Pharmaceutical Industry.