As a Clinical Supply Chain Manager, you will shape and drive the end-to-end supply strategy for new clinical trials, ensuring seamless study execution and meeting 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 (e.g. Annex 13).
- Create and maintain demand forecasts and packaging plans.
- 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.
- Maintain 100% compliance on all assigned training and applies learnings to everyday practice.
- 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.