Job Detail

Supply Chain Project Manager (Clinical Trials)

Inseriert am: 17.05.2018
:Job Description


When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

Fisher Clinical Services GmbH is part of Thermo Fisher Scientific Corporation, a world-class company serving the scientific community and healthcare industry. We are leaders in providing clinical supply chain management services and clinical supplies distributed to patients worldwide. For more information about our site in Allschwil please visit: www.fisherclinicalservices.com

For our CSOS team (Clinical Supply Optimization Service) in Allschwil/Basel we are looking for a

Supply Chain Project Manager (Clinical Trials)

The Supply Chain Project Manager is responsible for the Organization of a Clinical Trial from the Set Up Phase during the Maintenance Phase till Close Out Phase. This position will work with FCS (Fisher Clinical Services GmbH) clients to understand the supply chain requirements to support clinical trials.

Your tasks:



  • 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

  • Ability to pull together a cross-functional team for study management activities

  • Designs and implements plan to supply study drug to global clinical trials using sound supply chain techniques

  • Ability to proactively manage a program of work, supply of medication, and manage risk management activities

  • 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

  • Works with FCS sales to coordinate a full-service approach with prospective clients


Your profile:



  • Bachelor’s degree or equivalent required. Degree in operations management or science-related field (equivalent work experience may be considered)

  • 2 years of experience in the pharmaceutical or clinical supply area

  • Certified in Project Management is preferred

  • Expertise in clinical trial supply chain management, including managing complex clinical trials globally is a plus

  • Exemplary communication skills in English. German is a plus

  • Exemplary computer skills, including high proficiency in Microsoft Excel (Macros) and Access

  • Exemplary teamwork and interpersonal skills

  • Strong organizational and self-management skills


What We Offer:



  • Employment with an innovative and future-oriented organization

  • Outstanding career and development prospects

  • Company pension scheme

  • Exciting company culture which stands for integrity, intensity, involvement and innovation



At Thermo Fisher Scientific, each one of our 65,000 extraordinary minds has a unique story
to tell. Join us and contribute to our singular mission—enabling our customers to make the
world healthier, cleaner and safer.
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