.About the RoleStep into a world where your expertise in clinical vendor management becomes the catalyst for advancing medical breakthroughs.As a Clinical Trial Vendor Manager, you'll play a key role in our clinical operations, ensuring that every vendor interaction accelerates our journey towards new healthcare solutions.Key Responsibilities :Protocol Precision : Review vendor-related sections of the protocol, leveraging vendor expertise to refine specifications and achieve the perfect Final Protocol.Strategic Sourcing : Play a key role in crafting the Study Specification Worksheet (SSW), leading the bid process, and selecting top-notch vendors who align with our vision.Financial Finesse : Oversee the financial aspects with a keen eye, from analyzing quotes / proposals in collaboration with procurement to managing vendor budgets and ensuring accurate invoice reconciliation.Operational Excellence : Provide comprehensive program support by understanding and supplying study demands, ensuring submission documents are complete, and maintaining alignment with site requirements for successful study participation.Dynamic Collaboration : Work in tandem with trial and monitoring teams, procurement, and vendors to ensure a harmonious start-up, resupply, and close-out of studies.Quality Leadership : Uphold service excellence at the study level, acting as an escalation point for queries and ensuring vendors meet our high standards of quality and service.Risk Management Guru : Proactively develop and maintain vendor-related risk maps, complete with contingency plans, and follow up on any risks or issues with precision and care.Innovative Problem-Solving : Drive the analysis of supplier performance issues, identifying trends and implementing corrective actions to continuously improve vendor relations.Process Optimization : Support the implementation and amendment of vendor contracts, standards, templates, tools, and processes, ensuring a streamlined and efficient vendor management system.Technology Integration : Utilize the Unified Vendor Portal (UVP) to manage vendor service delivery, fostering a tech-savvy approach to vendor oversight.Continuous Improvement : Partner with practice leaders on improvement projects, contributing to learning loops and enhancing vendor qualification processes.Educational Development : Collaborate with vendors to develop and refine training materials, ensuring site and monitor readiness through active participation and support.What We're Looking For :Regulatory Expertise : Deep knowledge of clinical research regulations, including GCP and ICH guidelines, with the ability to apply them in a practical setting.Therapeutic Wisdom : A broad understanding of clinical protocols and therapeutic areas, ensuring meticulous attention to detail in every aspect of the role.Experience with Radioligand Therapy in Oncology studies is a must
