Jason

About Jason

A clinical supply chain professional, with over nine years of pharmaceutical expertise including drug product manufacturing and quality assurance. Proficient in project management, GMP technical operations, and external vendor management. Known to communicate effectively with internal cross functional stakeholders. Excels in establishing and executing project deliverables, adapting within dynamic work environments, and continuing to improve existing procedures.

Experience

1. Senior Manager, Clinical Supply Chain

   Sumitomo Pharma America, Inc.

   Oct 2023 — Present · Marlborough, MA, US

   Serve as lead clinical supply manager for multiple early and late phase programs, by creating bulk tablet and finished good supply plans to identify total study drug demand, forecast, and overage amounts through study protocol interpretation.• Perform monthly on-hand inventory review by adjusting actuals of study specific and bulk drug product supply and demand models, contributing to having adequate drug, IP waste reduction, and adhering to or reducing spend of program budgets.• Oversee domestic and global site and depot distribution for multiple clinical studies, post study access programs, and for production related stability samples, by working with external vendor project managers to ensure on time delivery of supplies.• Manage primary and secondary packaging and labeling operations of investigational products, including assessment of raw britestock materials, clinical label design, master text translation, and production schedule management of finished goods.• Initiate depot close out activities by requesting vendors for depot inventory and site returns reports to conduct material accountability and destruction of excess supplies, helping to minimize spend on storage and project management fees.• Establish study level and DP demand timelines by partnering with functional leaders in CMC, Clinical Operations, Project Management, and Regulatory Affairs, enabling that study start up deliverables and program requirements are met.• Provide IRT support with study teams, serving as a supply manager by participating in new system builds and UAT, reviewing specification requirements, monitoring drug expiry, initiating inventory release, and generating manual shipments.• Support and manage third party relations with vendors by identifying and selecting providers based on study needs, initiating RFPs, reviewing invoices, and managing purchase orders, through working with internal business operations.

Education

• University of California, Davis

  Bachelor of Science - BS, Biotechnology

• The Johns Hopkins University

  Master of Science - MS, Regulatory Science

Skills

• Protein Purification
• Dna Extraction
• Rna Extraction
• Plasmid Isolation
• Sds-Page
• Agarose Gel Electrophoresis
• Western Blotting
• Pcr
• Qpcr
• Plant Transformation
• Dna
• Pipetting
• Plant Maintenance
• Greenhouse
• Data Entry
• Microsoft Word
• Microsoft Excel
• Blast Analyses
• Mass Spectrometry
• Column Chromatography
• Cell Culture
• Research
• Molecular Biology
• Public Speaking
• Biotechnology
• Microsoft Office
• Polymerase Chain Reaction (Pcr)
• Real-Time Polymerase Chain Reaction (Qpcr)
• Clinical Trials
• Clinical Supplies
• Supply Chain Management
• Quality Assurance
• Gmp
• Standard Operating Procedure (Sop)
• Project Coordination