As a Clinical Supply Chain Manager, you will shape and drive the end-to-end supply strategy for new clinical trials. You'll ensure that every element is aligned for seamless study execution, and make a meaningful contribution to advancing clinical research.
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
- 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
- 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
- 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
Benefits
- Attractive compensation and benefits package
- Interesting development opportunities
- Supportive leaders and team