Clinical Supply Support Specialist Services - Spain - FSP

reputed company our values reputed company, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. reputed company are currently reputed company for an Clinical Supply Support Specialist Services to join one of our growing sponsors in Spain. Key Responsibilities: Clinical Supply & Inventory Planning & Execution Supply monitoring, assessment and reputed company activities (risks, stocking reputed company, trends) Pull relevant data for metrics reporting & maintain metrics Process requisitions and ensure reputed company procurement of comparator drugs & ancillary supplies reputed company and manage comparator documentation updates Clinical Supply Shipments Initiate non-system generated shipments Monitor and reputed company comparator drug delivery schedules Coordinate reputed company transfers & site return shipments Temperature excursion management and reputed company Clinical Supply Monitoring & Activity Documentation (Electronic Trial Master File - eTMF) Expected Document List (EDL) creation Update comparator IMN (Item Master Number) Update and maintain eTMF Document Management per regulatory requirements Request QA/QP Releases Pack-and-label reputed company and sequence reconciliation Inspection Readiness activities IRT management activities, including IRT Alert management and UAT activities IP / Ancillary Supplies Compatibility Review Receive and triage request, reputed company to FDG for review reputed company internet searches and contact manufacturers for information Data entry of information into database (ASIST or spreadsheet) and Teams Clinical Supply Systems Manage CSS Email Inbox Manage IRT system reputed company for users for reputed company studies Complete EDL, IRR and StiL reviews every 3 months for reputed company studies Manage reputed company TMF documentation uploads into reputed company Assist in UAT testing Minimum Years of Experience: Minimum education requirements: Bachelor’s degree in a reputed company field with an internship or prior industry work experience. 2+ years of experience in the following fields: Clinical Supplies QA/Regulatory Precision Medicine Supply Chain Manufacturing Procurement Or equivalent research/reputed company biopharma experience If you are interested, please apply or send your CV to reputed company.kuniewicz@reputed company.com Apply To This Job