Global Clinical Supply Chain Lead

IQVIA; Paris; Sur place; EUR 70 000 - 110 000; Plein temps

Résumé du poste

IQVIA in Paris is seeking a Clinical Supply Chain Manager to shape the end-to-end supply strategy for new clinical trials. You will translate study protocols into robust supply plans and ensure alignment with timelines and quality standards.

Collaborating with internal teams and external partners, you will drive forecasting, packing campaigns, budget tracking, and regulatory compliance to support efficient study execution.

Qualifications

• Bachelor's Degree in science or business (preferred, not essential).
• 3–5 years experience in Clinical Trials (essential).
• 3–5 years experience in Clinical Supply Chain Management (essential).
• Proven project management skills.
• Ability to build working relationships with stakeholders.
• Strong communication and leadership abilities.
• Proficient in English.

Responsabilités

• Interpret clinical trial protocols to design and execute a clinical trial supply chain solution.
• Create master English label text per regulatory requirements (e.g., Annex 13).
• Develop demand forecasts and packaging plans to ensure timely availability of materials.
• Lead packaging campaigns with vendors and oversee on-time delivery.
• Manage IRT systems to track study inventory and distribution plans.
• Provide budgeting oversight aligned with quotations and client approvals.
• Maintain GxP compliance and regulatory knowledge relevant to the role.
• Lead client/vendor meetings on supply chain topics and updates.

Connaissances

Project management

Stakeholder management

Analytical thinking

Communication skills

Problem solving

English language proficiency

Regulatory compliance awareness

Formation

Bachelor's Degree in Science/Business

Outils

Microsoft Office Suite

Description du poste

IQVIA in Paris is seeking a Clinical Supply Chain Manager to shape the end-to-end supply strategy for new clinical trials. You will translate study protocols into robust supply plans and ensure alignment with timelines and quality standards.

Collaborating with internal teams and external partners, you will drive forecasting, packing campaigns, budget tracking, and regulatory compliance to support efficient study execution.