Clinical Supply Chain Manager
2 semanas atrás
Job Overview
The Clinical Supply Chain Manager is responsible for managing the strategic planning and execution of clinical supply chain projects. This role will support the ongoing development and optimization of the Clinical Trial Supplies department and processes.
Key Responsibilities- Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution.
- Create master English label text in accordance with relevant regulatory framework.
- Create and maintain demand forecasts and packaging plans to ensure packed clinical supplies are readily available in accordance with project requirements.
- Initiate packaging campaigns with assigned vendors and provide oversight to ensure timely delivery.
- Setup, monitor, and update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed.
- Create an appropriate distribution plan and have oversight of assigned vendors executing it.
- Ability to work independently and proactively to ensure the supply of all trial materials is delivered to the right place at the right time.
- Provide ongoing budget tracking activities to ensure projects are run efficiently and in accordance with client-approved quotations.
- Maintain 100% compliance on all assigned training and apply learnings to everyday practice.
- Remain up to date in all GxP and regulatory requirements applicable to the role.
- Lead client and vendor-related meetings where necessary to discuss clinical supply chain topics or status updates.
- Create a Temperature Excursion management plan.
- Manage the review and assessment process of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team.
- Conduct thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed.
- Support client bid defense meetings as required.
- Support the development and optimizations of the CTS department and processes.
- Bachelor's Degree in a science or business function (Preferred not essential).
- 2-3 Years industry experience in Clinical Trials (Essential).
- 2-3 Years experience in Clinical Supply Chain Management (Essential).
- 2-3 Years with IRT systems.
- Ability to demonstrate good project management skills.
- Ability to create effective working relationships with internal and external stakeholders.
- Ability to demonstrate effective communication and direction.
- Ability to problem solve.
- Strong Microsoft Office skills (Word, Excel, PowerPoint, etc).
- Proficient in the English language.
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