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Associate Clinical Supply Chain Director
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Full-time
- The AD partners with other functional leaders in CMC, Regulatory Affairs, Clinical Operation and Quality Assurance in support of the study project teams and ensures timely drug supply for clinical trials.
- Create global supply strategies, supply plans to support clinical studies; collaborate with Pharmaceutical Operations, Clinical Operations, Regulatory Affairs, Quality Assurance, and external vendors to execute the strategies for the clinical studies.
- Manage label development process from generation of the master label text to label printing.
- Lead the development, review and User Acceptance Testing (UAT) of the Interactive Response Technology (IRT) system.
- Utilize appropriate software and IT systems (e.g. IRT, MS Office, MS Project, Smartsheets, and others) to effectively manage key project activities.
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