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Responsible and accountable for the ordering, receiving, processing, storing, shipment and delivery, return drug accountability, reconciliation and destruction of clinical supplies returned by the clinical sites of drug products and medical devices for assigned studies. Performs local purchases activities as per request.
Responsible for logistics coordination of low to moderately complex studies.
This position primarily ensures the day to day operations and management of the local/in country clinical supply activities in accordance with all contracted services, applicable regulatory requirements and laws, and sponsor/PPD policies and procedures.
**Education and Experience**: Bachelor's degree in a pharmacy or related discipline.0-1 year of clinical supplies project coordination experience or equivalent GMP experience.Acceptable knowledge of cGMP, GDP, GCP, and ICH knowledge is essential.Familiar with clinical supply terminology and practices and principles. Knowledge, Skills and Abilities: Adequate knowledge of the complete clinical supplies life cycle (i.e., manufacturing, packaging, labeling, import and export, storage and handling, distribution and delivery, return and reconciliation, final destruction).Focus on Customer Service aligned with highest standards of quality and excellence.Strong organizational skills required.Very strong communication skills both written and verbal.Fluent in English (verbal and written).Strong computer skills: working knowledge of Microsoft Project, Excel, and Microsoft Word is required.PPD is an Equal Opportunity Employer
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