Clinical Supply Chain

As a Global Study Supply Support (GSSS) in our company, you will play a crucial role in providing operational support to Clinical Supply Chain Study Leaders for multiple studies across all phases. Your responsibilities will include working independently and collaborating with multiple leaders and cross-functional teams, preparing and tracking transfer orders, managing stock reconciliation, performing quality checks, preparing documentation for labeling and shipments, monitoring needs for destruction, and archiving documents in the electronic Trial Master File. Your key responsibilities will involve supporting clinical supply chain operations for global studies, ensuring compliance with regulatory standards and protocols, maintaining accurate documentation and inspection readiness, and effectively communicating with supply chain leaders, operational teams, and outsourcing partners. You must also be adaptable to changing priorities in a fast-paced environment. To excel in this role, you must possess a Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD), have experience in clinical supply support or logistics for clinical trials (Phase I-IV), be proficient in digital tools and supply chain software, have knowledge of regulatory standards (quality, safety, documentation), and be familiar with investigational product management including kit types, shelf life, depot management, distribution, reconciliation, returns, and destruction. Additionally, proficiency with tools such as IRT (e.g., Endpoint, Suvoda), Smart Supplies, Veeva Vault, documentation and quality check skills, as well as fluent English for communication with stakeholders are essential. Your success in this role will be driven by your attention to detail and organizational skills, ability to manage multiple priorities and work collaboratively in a multicultural environment, strong problem-solving and adaptability skills, and comfort with digital tools and documentation processes.,