- Thermo Fisher Scientific
101 Olde Field Rd
Position Summary: Working independently or with members of a Clinical Ancillary Management project team, the Clinical Ancillary Supply Chain Manager is responsible to ensure timely availability of clinical study materials and ancillary supplies to Fisher Clinical Services distribution depots, customer affiliates, and/or investigator sites globally. This includes collaborating with customers and internal resources to define requirements, developing plans and timelines, and coordinating and executing project activities ?
How will you make an impact? Responsible for understanding the core clinical trial study requirements, including relevant details which will shape ongoing study decisions. Leverages in-depth background of the therapy (e.g. diabetes) associated with the clinical trial and clinical processes (e.g. clinical packaging) to proactively recommend ancillary strategies which facilitate the successful outcome of the study. Responsible for coordinating with Sales to learn all study requirements and handoff project following client awarded. Responsible to create and adapt all elements of project plan for complex studies including, scope, communication plan, cross-functional / global support requirements, risk management plan, schedule etc. Acts as single point of contact for client and coordinates key activities with other FCS functions as required (e.g. packaging). Ensures all support resources understand their roles and are committed to supporting the study according to plan. Responsible to create and modify the demand and supply plan tool for complex global studies based on client requirements and study changes. Execute work by utilizing approved tools and processes. Responsible to set up and modify complex global jobs in the project management system (GPM) . Information includes, Purchase requisitions, IL Information/export information. Other items include ensuring all distribution information is communicated to all depots, for example quotes are sent, country of manufacturing, pricing etc. How will you get here? Education: Bachelor's Degree in business or science related field or equivalent experience Minimum Requirements: Minimum of 5-7 years of project management and clinical supplies, healthcare, or medical device Ability to work as part of a cross-functional team for study management activities. Creates an environment to optimize team performance.\\\\ Exemplary computer skills, including high proficiency in Microsoft Suite including Excel, Word and MS Project as well as the Office 365 environment. Ability to analyze complex data and make informed decisions Strong communication skills and attention to detail. Ability to have difficult conversation both internally and with clients Strong organizational and self-management skills. Ability to prioritize complex tasks in matrix environment Experience working in GxP regulated environment, ISO, or other heavily regulated environment Preferred Qualifications: Certified Project Management Professional is preferred. APICS certification (CPIM) also desirable.
Responsible for creating, interpreting and maintaining complex supply chain strategies of complex ancillary studies. Must have the ability to create and execute project plan which coordinate all activities of teams that support CAM in all areas around the world. Must have the ability to support with Packaging, labeling and comparator needs In addition is responsible for collaborating with clients and sales to tailor FCS services to emerging client needs. Also assists other CAM employees with technical / process questions and collaborates with leadership team to drive best practices and standardize processes across the business.
What will you do?
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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
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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.
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* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.
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