Role overview
Supports supply chain for global clinical trials. Ensures project/study activities are in compliance with company and client requirements.
A day in the life
- Develops study specific plans for each assigned project.
- Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets.
- Ensures fluent communication and interaction between internal departments in order to avoid obstacles during the course of the study.
- Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.
- Participates in ongoing training on new regulations
Education and Experience:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
