Clinical Supply Chain Manager

4 weeks ago

Oxford, Oxfordshire, United Kingdom Psi CRO Ag Full time
Job Title: Clinical Supply Chain Manager

We are a dynamic, global company that brings together passionate individuals to work on the frontline of medical science. Our mission is to change lives and bring new medicines to those who need them.

Job Description

In this role, you will oversee all Supply Chain Management activities within large, complex clinical studies or programs. Your primary responsibility will be to ensure the timely and efficient delivery of clinical supplies to investigative sites.

Key Responsibilities:

  • Coordinate and supervise Supply Chain Management activities within small to medium-sized clinical studies
  • Assess and/or setup trial supply schemes involving distribution depots and investigative sites, and interactive response technology
  • Plan the optimal campaign strategy to ensure clinical supplies are available in accordance with project requirements
  • Oversee and/or lead setup, testing, and ongoing monitoring of interactive response technology systems as well as IMPs and NIMPs supply activities
  • Manage the IRT vendor, leading study-specific system setup, UAT, system acceptance, and ongoing system updates
  • Develop the clinical supply management plan and provide input to vendor management plans regarding procurement and/or secondary manufacturing, distribution, and interactive response technology systems
  • Participate in the selection of trial supply vendors and IRT vendors for PSI studies
  • Support and train PSI teams in clinical supply management
  • Liaise with PSI project teams, company divisions, clients, and vendors
  • Assess risks associated with clinical product management and quality incidences reported by vendors
  • Support business development tasks related to clinical trial supply services
Requirements
  • College or University degree
  • 3-5 years experience in Clinical Supply Chain Management (Essential)
  • Experience working with supply chain technologies (i.e. IRT, CTMS, IWRS integration rules and principles)
  • Training in GMP and GDP
  • Ability to communicate effectively with vendors and internal parties
  • Ability to work both independently and in a team environment
  • PC skills to be able to work with MS Word, Excel, and PowerPoint

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