ironquill.tech/board

$ cat jobs/clinical-supply-chain-manager-lifelancer-f0f48fd87fee.json

Clinical Supply Chain Manager

lifelancer·US·United States·mid
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Job Title: Clinical Supply Chain Manager Job Location: Sao Paulo, Brazil Job Location Type: Home-based Job Contract Type: Full time Job Seniority Level: Clinical Supply Chain Manager Full home-based Job Overview The Clinical Supply Chain Manager is responsible for the strategic planning and execution of new clinical trial supply chains. This involves the ability to interpret a clinical trial protocol in conjunction with other key study information in order to create an appropriate kit design and formulate a strong supply plan. Essencial functions • Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution • Create master English label text in accordance with relevant regulatory framework • Create and maintain demand forecasts and packaging plans so that packed clinical supplies are readily available in accordance with the project requirements • Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery • Setup, monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed • Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it • Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations • Maintains 100% compliance on all assigned training and applies learnings to everyday practice • Remain up to date in all GxP and regulatory requirements applicable to the role • Leads client and vendor related meetings where necessary to discuss clinical supply chain topics or status updates • Creates a Temperature Excursion management plan • Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed Requirements High School Diploma or equivalent 2-3 Years related industry experience in Clinical Trials 2-3 Y