Sr Associate Clinical Finish Drug Product Global Study Planner Support

Lets do this. Lets change the world. In this vital role, you will serve as lynchpin between Global Study Planners and internal and external customers to ensure supply for our important patients participating in Amgens global clinical trials. Along with local team members, you support the execution of clinical planning processes and ensure the execution of activities so that Finished Drug Product is available from study start throughout study closure. You closely interact with Global Study Planners in Europe and USA.

Reporting to the Manager Clinical Finish Drug Product and Comparator Supply, you support the global execution of clinical planning processes. While the Global Study Planner decides the need for sufficient inventory and timely destruction, you execute on these requests. Each day you handle the requests for new labeling jobs in ERP based on the system signals. Another task is to initiate and follow up stock transfer orders in ERP in close conjunction with the planners information for quantity, timing and destination. You initiate the destruction of finish drug product and follow up in case of delays or discrepancies. You are also responsible for several periodic checks and give input to KPIs. You route controlled documents and update text after review workflow in conjunction with the subject matter expert.

The role is accountable for executing complex supply chain processes, accurate, timely and GMP compliant execution and follow up. You provide operational oversight across supply planning, order management, material destruction and indicate problems and inconsistencies. In close collaboration with your local peers, you give support to the Global Study Planners based in other parts of the world. You manage workload prioritization and participate in performance management, risk mitigation, and continuous improvement initiatives across the teams, ensuring alignment with the global clinical supply chain priorities, regulatory requirements, and financial objectives.

Must-Have Skills:

Demonstrated accurate and efficient handling of process execution in a complex environment Strong problem solving and analytical skills towards driving robust decision making Good organizational and communication skills including fluency in English both in oral and written communication with the ability to clearly document and communicate relevant information. Demonstrated ability to manage assigned tasks and priorities while meeting deadlines. Ability to adapt to evolving priorities that clinical studies that are agile by nature. Hands-on knowledge of SAP or similar ERP system for material planning and management. Ability to work effectively within cross-functional teams in a regulated or structured environment. Collaborative team player with the ability to support shared objectives. Experience or exposure to working with stakeholders in other time zones. Basic understanding of performance metrics, reporting tools, or data tracking processes.