Job Summary
Performs administrative and support activities, as assigned by the Clinical Trial Supplies Manager (CTSM) or Project Lead (PL), to help manage the logistics of clinical trial supplies (e.g., batch review, customs clearance, supply and return). Job Responsibilities
Performs administrative and support activities, as assigned by the Clinical Trial Supplies Manager (CTSM) or Project Lead (PL), to help manage the logistics of clinical trial supplies (e.g., batch review, customs clearance, supply and return). Job Responsibilities
- Assists in the development of systems and plans for distribution, re-supply, and return of clinical trial supplies.
- Supports the review of batch manufacturing and packaging records to enable batch disposition.
- Supports review and forecasting of inventory levels for all clinical trial supplies, in cooperation with project teams and project vendors
- Associate’s Degree (or equivalent) level of education, preferably focused on life sciences
- Experience in a contract research organization (CRO), pharmaceutical, or biotechnology company preferred
- Knowledge of Good Clinical Practice, ICH guidelines, Good Manufacturing Practice, and other applicable regulatory requirements
- High level of competence in English language
- Proficiency with MS Office Applications
- Ability to travel as necessary (up to 5%)
Vacancy posted 14 days ago
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