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Supplier coordinator - FSP

Primary Location: United Kingdom, Remote ID de la oferta R0000041249 Categoría Administrative
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Key Responsibilities:

Clinical Supply & Inventory Planning & Execution

  • Supply monitoring, assessment and oversight activities (risks, stocking levels, trends)

  • Pull relevant data for metrics reporting & maintain metrics

  • Process requisitions and ensure timely procurement of comparator drugs & ancillary supplies

  • Track and manage comparator documentation updates

Clinical Supply Shipments

  • Initiate non-system generated shipments

  • Monitor and track comparator drug delivery schedules

  • Coordinate Depot transfers & site return shipments

  • Temperature excursion management and resolution

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 kit 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, forward to FDG for review

  • Perform 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 access for users for all studies

  • Complete EDL, IRR and StiL reviews every 3 months for all studies

  • Manage all TMF documentation uploads into VEEVA

  • Assist in UAT testing

Minimum Years of Experience:

Minimum education requirements:

Bachelor’s degree in a related 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/commercial biopharma experience


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