Project Management,Packaging,GMP,Quality,Clinical Trial
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About The Position
The position involves supporting the clinical supply project manager in the planning, scheduling, coordination, and execution of tasks to ensure the timely availability of investigational drug supplies and related services to clinical sites and depots. The role requires translating stability and packaging requests into executed packaging designs, as well as identifying, developing, communicating, and tracking task completion dates, activities, logistics, and milestones. This is crucial for ensuring that investigational drug supplies are available when needed. Additionally, the candidate will be responsible for creating appropriate protocol-specific manufacturing and packaging work orders in collaboration with the clinical supply project manager. The role also includes completing tasks identified for the team and setting up inventory management systems to support clinical packaging operations. A basic understanding of clinical development and global supply chain requirements is essential, along with the ability to apply standard business requirements such as SOPs and global regulations. The candidate must understand the importance of compliance in a regulated environment and be capable of applying this knowledge to daily work. Effective collaboration within the department and cross-functionally is necessary, as well as the ability to manage and prioritize multiple tasks. Good communication skills, both written and oral, are also required for this role.
