As a Clinical Supply Chain Manager, you will shape and drive the end-to-end supply strategy for new clinical trials. You will ensure that every element is aligned for seamless study execution. The role involves collaboration with internal teams and external partners to deliver a supply chain that meets highest quality standards and study timelines.
Requirements
- 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.
- Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery.
- Setup, monitor, and update study assigned Interactive Response Technology (IRT) systems.
- Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it.
- Provide ongoing budget tracking activities.
- Maintains 100% compliance on all assigned training and applies 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.
- Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed.
Benefits
- Attractive compensation and benefits package
- Interesting development opportunities
- Supportive leaders and team