Clinical Supply Support Specialist Services - 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 FSP is hiring multiple Clinical Supply Support Specialist Services. 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 education requirements: Bachelor’s degree in a reputed company field with an internship or prior industry work experience. Preferred 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

Apply To This Job