Strategic Clinical Trial Supply Chain Lead

IQVIA Argentina; Paris; Sur place; EUR 70 000 - 100 000; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Supply Chain Manager in Paris to shape end-to-end supply strategy for new clinical trials. You will translate complex study protocols into robust kit designs and supply plans, ensuring alignment for seamless study execution.

Collaborate with internal teams and external partners, lead planning and delivery with high quality standards and timelines; drive budget tracking and regulatory compliance, including GxP knowledge.

Qualifications

• 3–5 years in Clinical Trials.
• 3–5 years in Clinical Supply Chain Management.
• Strong communication and project management skills.

Responsabilités

• 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 so that packed clinical supplies are readily available in accordance with the project requirements.
• Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery.
• Setup, monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed.
• Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it.

Connaissances

Project management

Stakeholder management

English proficiency

MS Office

Formation

Bachelor's Degree in science or business

Outils

Microsoft Excel

Microsoft PowerPoint

Description du poste

IQVIA is seeking a Clinical Supply Chain Manager in Paris to shape end-to-end supply strategy for new clinical trials. You will translate complex study protocols into robust kit designs and supply plans, ensuring alignment for seamless study execution.

Collaborate with internal teams and external partners, lead planning and delivery with high quality standards and timelines; drive budget tracking and regulatory compliance, including GxP knowledge.