Clinical Supply Chain Manager临床试验供应链

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. The Clinical Supply Chain Manager will lead internal and external partners, to ensure delivery of the supply plan in accordance with study timelines.
Essential 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 (e.g. Annex 13)
● 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
● Ability to work independently and proactively to ensure that the supply of all trial materials is delivered to the right place at the right time
● 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
● Manages the review and assessment process of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team
● Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed
Qualifications
● Bachelor's Degree Degree in a science or business function (Preferred not essential) Req
● 2-3 Years related industry experience in Clinical Trials (Essential).
● 2-3 Years experience in Clinical Supply Chain Management (Essential).
● Ability to demonstrate good project management skills.
● Ability to create effective working relationships with internal and external stakeholders.
● Ability to demonstrate effective communication and direction.
● Ability to problem solve.
● Strong Microsoft Office skills (Word, Excel, Powerpoint etc).
● Proficient in the English language.
全国居家办公
4-5年临床试验供应链相关经验
英语可作为工作语言。