Global Study Supply Support

Role Overview: As a Clinical Supply Chain Support Specialist at Capgemini, you will provide operational support to Clinical Supply Chain Study Leaders for multiple studies across all phases (set-up, follow-up, closure). You'll work independently and collaborate with cross-functional teams to ensure smooth supply chain operations and compliance with regulatory standards. Key Responsibilities: - Prepare and track transfer orders. - Manage stock reconciliation and monitor destruction needs. - Perform quality checks and maintain inspection readiness. - Prepare documentation for labeling and shipments. - Archive documents in the electronic Trial Master File. - Communicate effectively with supply chain leaders, operational teams, and outsourcing partners. - Adapt to changing priorities in a fast-paced environment. Qualifications Required: - Education: Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD). - Experience in clinical supply support or logistics for clinical trials (Phase IIV). - Knowledge of regulatory standards (quality, safety, documentation). - Understanding of investigational product management (kit types, shelf life, depot management, distribution, reconciliation, returns, destruction). - Technical Skills: Proficiency with tools such as IRT (e.g., Endpoint, Suvoda), Smart Supplies, Veeva Vault. - Strong documentation and quality check skills. - Language: Fluent English for communication with stakeholders. Additional Company Details: Capgemini is a global business and technology transformation partner, helping organizations accelerate their dual transformation to address the evolving needs of customers and citizens. With a strong 55-year heritage and deep industry expertise, Capgemini is trusted by its clients to address the entire breadth of their business needsfrom strategy and design to operations. The organization values flexibility, inclusivity, and continuous learning opportunities for its employees to excel in a diverse and innovative environment.,