**Associate Clinical Supply Chain Manager - Ancillaries****EMEA - Remote**When you join us at Thermo Fisher Scientific, you’ll be part of an inquisitive team that shares your passion for exploration and discovery. With revenues of more than $40 billion and the largest investment in R&D; in the industry, we give our people the resources and chances to create significant contributions to the world.**Location/Division Specific Information**As an Associate Clinical Supply Chain Manager, you will ensure timely availability of clinical study materials to Fisher Clinical Services (FCS) distribution depots, customer affiliates, and/or investigator sites, globally. This includes collaborating with customers and internal resources to define requirements, develop plans and timelines, and coordinating and impactful project activities.**Your Key Responsibilities**- Implement and follow defined distribution plan to supply Clinical Ancillary Materials to global clinical trials, using sound supply chain techniques.- Act as a single point of contact for clients and coordinate key activities with other FCS departments.- Build new demand and supply plans for simple studies using approved tools and processes.- Proactively identify potential supply chain issues, providing analysis and recommending solutions- Ensure changes are communicated promptly to all cross functional and resources to ensure all phases of execution align with the plan.- Understand high level import/export requirements for global distribution and ensure the appropriate distribution team members are involved to generate required documentation and to ensure appropriate procedures are in place.- Lead study close-out activities including returned good reconciliation, inventory destruction processing, and file archiving- Stay on top of relevant cGMPs, GCPs, and other regulatory requirements and ensure study management activities are aligned.- Demonstrate and promote the company vision.- Conduct activities in a safe and efficient manner**Education**- Bachelor’s degree or higher in operations management or science-related field (equivalent work experience may be considered)- Minimum of 3 years of Project management experience within either clinical supplies, healthcare, or medical devices - clinical trial knowledge and experience, highly preferred**Experience**- Experienced in efficiently and proactively managing projects.- Experience working in GxP regulated environment, ISO, or other heavily regulated environment.**Knowledge, Skills, Abilities**- Project Management professional certification is an advantage- Exemplary digital literacy, including high proficiency in Microsoft Suite including Excel, Word and MS Project as well as the Office 365 environment.- Ability to analyze sophisticated data and make informed decisions. Requires intermediate skills level for spreadsheets.- Excellent Collaboration and interpersonal skills with the ability to work within a cross-functional and general team- Strong oral and written communication skills- Accuracy and attentiveness to details- Ability to identify problems and work toward a solution- Ability to independently balance priorities and workday in a remote setting- Travel will rarely be required (0-10%)Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.**Accessibility/Disability Access