In this vital role, you will serve asSr Associate, supporting the Design and Setup of the Clinical Supply Chain.
Reporting to theManager Clinical Supply Chain-Change Mgt,anddirected by the Global Setup Leads,you willcontribute to theexecution and completion of key deliverables associated withsetup activities of global supply chains for clinical trials, by leading information gathering across stakeholderssuch as R&D, Regulatory Affairs, Site Supply Chain and Master data, and task close out.
In close collaboration withthe Global Setup Lead team,you will ensure reliable, compliant, and right-first-time process execution,transparentstatus reporting on progress, andpro-activeidentification of risks and mitigation strategiesfor closing out deliverables.
The role is accountable formanagingvarious deliverablessuch as:
Master data requests forproduct materials,Bill of Materials (BOM), and study related attributes in SAP.
Creation of the Clinical Artworkrequestsandfacilitatingprioritization of outstandingattributes in relation to the request form.
Creationand maintenance of Product Specification Files, and Depot Plans.
Requesting Finished Drug Product Materials, Bill of Materials (BOM), Work Breakdown Structure (WBS) elements, Custom Values and ensurestimelyavailability to adhere to overall project timelines
