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Job ID :
44124BR
Location :
US - California - Remote / Field|US - Alabama - Remote / Field|US - Alaska - Remote / Field|US - Arizona - Remote / Field|US - Arkansas - Remote / Field|US - Connecticut - Remote / Field|US - Florida - Remote / Field|US - Georgia - Remote / Field|US - Illinois - Remote / Field|US - Indiana - Remote / Field|US - Kansas - Remote / Field|US - Louisiana - Remote / Field|US - Massachusetts - Remote / Field|US - Michigan - Remote / Field|US - New Jersey - Remote / Field|US - New Mexico - Remote / Field|US - New York - Remote / Field|US - North Carolina - Remote / Field|US - Ohio - Remote / Field|US - Oregon - Remote / Field|US - Pennsylvania - Remote / Field|US - South Carolina - Remote / Field|US - Tennessee - Remote / Field|US - Texas - Remote / Field|US - Utah - Remote / Field|US - Vermont - Remote / Field|US - Virginia - Remote / Field|US - Washington D.C. - Remote / Field|US - West Virginia - Remote / Field|US - Wisconsin - Remote / Field|US - Wyoming - Remote / Field
:
Job Description

Responsibilities:

  • Demonstrates ability to promote the company vision
  • Utilizes an extensive network in the pharmaceutical industry to generate and cultivate leads for the CSOS
  • Works with FCS sales to coordinate a full-service approach with prospective clients
  • Utilizes understanding of Clinical Trial Supply Chain Management best practice principles to develop new or improve existing business processes and appropriately document and revise or develop associated training materials
  • Effectively mentors and coaches associates new to the CSOS role on best practices associated with managing clinical supply chains
  • Designs and implements plan to supply study drug to global clinical trials using sound supply chain techniques
  • Devises and implements inventory management plans that have complex supply chains
  • Leverages the inventory management capabilities of the Interactive Response Technology (IRT) to appropriately manage studies
  • Stays abreast of relevant cGMPs, GCPs, and other regulatory requirements and ensures study management activities are aligned
  • Attend relevant client-related meetings and appropriately represent status of the Clinical Supply Chain
  • Conduct activities in a safe and efficient manner
  • Other duties may be assigned to meet the needs of the business

Minimum Qualifications:

  • Bachelor’s degree or equivalent required. Degree in operations management or science-related field (equivalent work experience may be considered
  • 5-6 years of experience in the clinical supply area
  • Certificates: Certified Project Management Professional is preferred. APICS certification (CPIM) is also desirable
  • Minimum of three years clinical supply experience, either in Logistics and/or Packaging
  • Demonstrated experience with multiple global clinical trials
  • Expertise in clinical trial supply chain management, including managing complex clinical trials globally
  • Exemplary communication skills
  • Exemplary computer skills, including high proficiency in Microsoft Excel.
  • Exemplary teamwork and interpersonal skills
  • Strong organizational and self-management skills
  • Strong project management skills

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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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