- Coordinates the origination, proofing and transition of clinical study labels.
- Proactively communicates drug supply delivery timelines to appropriate stakeholders.
- Coordinates the required documentation and activities for import and export of clinical supplies.
- Monitors global inventory and proactively communicates with all stakeholders to ensure adequate quantity and timely delivery of clinical supplies throughout duration of a trial.
- Monitors and manages retest dating for assigned study supplies.
- Proactively identifies potential risks, provides corrective plans, and resolves clinical supply issues and complaints.
- Provides information to support financial planning for global studies and monitors drug supply study budget.
- Reviews new proposal requests and determines required clinical supplies management support.
- Provides responses to potential new client request for information related to clinical supplies management
Education and Work Experience:
- Bachelor degree required.
- Advanced degree nice to have.
- Drug Forecasting (Off the protocol preferred) or Demand Planning experience required.
- 3 plus years of prior experience in a pharmaceutical, biotech and clinical supply logistics environment preferred
Knowledge, Skills, and Abilities:
- Working knowledge of the Clinical Trial Supply process
