Clinical Supply Chain Manager

Thermo Fisher Scientific
07 Oct 2016
20 Oct 2016
Contract Type
About Thermo Fisher Scientific Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of $12 billion, we have approximately 39,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries. We create value for our key stakeholders through three premier brands, Thermo Scientific, Fisher Scientific and UnityTM Lab Services, which offer a unique combination of innovative technologies, convenient purchasing options and a single solution for laboratory operations management. Our products and services help our customers solve complex analytical challenges, improve patient diagnostics and increase laboratory productivity. Visit Job Description Job Title: Clinical Supply Chain Manager Reports To: Manager, Clinical Supplies Optimisation Service Group/Division: BSD Career Band: III Job Track: Professional Position Location: Horsham Number of Direct Reports 0 Position Summary: The CSCM is the key point of contact for oversight and monitoring of stock levels at all Clinical Trial sites. This position is responsible for delivery and success of the study. Key Responsibilities: Demonstrates ability to promote the company vision Work directly with all key stakeholders to ensure stock at sites Ability to pull together a cross-functional team for study management activities Ability to proactively manage a program of work, supply of medication, and manage risk management activities Conduct activities in a safe and efficient manner Other duties may be assigned to meet the needs of the business Minimum Requirements/Qualifications: Bachelor's degree or equivalent by experience Non-Negotiable Hiring Criteria: 3-5 years industry experience, preferably in Clinical Supplies Ability to interpret a clinical protocol and translate into a supply plan Ability to forecast work for client accounts Full understanding of Project and Supply Chain Management role Strong understanding of IRT Full understanding of clinical trial phases/designs and how this translates into the entire supply plan Full understanding of Annex 13 and GMP regulations and country regulations for clinical trials