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Clinical Supply Chain Manager

2 months ago

Oxford, Oxfordshire, United Kingdom Psi CRO Ag Full time
Job Overview

We are a dynamic, global Contract Research Organization (CRO) founded in 1995, dedicated to delivering high-quality services to our clients. Our team of over 2,700 passionate individuals works on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Key Responsibilities
  • Manage all Supply Chain Management activities within large, complex clinical studies or programs, ensuring seamless coordination and supervision.
  • Assess and/or setup trial supply schemes involving distribution depots and investigative sites, leveraging interactive response technology to optimize supply chain efficiency.
  • Develop and implement campaign strategies to ensure clinical supplies are available in accordance with project requirements, driving business growth and customer satisfaction.
  • Oversee and/or lead the setup, testing, and ongoing monitoring of interactive response technology systems, as well as the management of Investigational Medicinal Products (IMPs) and Non-Investigational Medicinal Products (NIMPs) supply activities.
  • Manage IRT vendors, leading study-specific system setup, User Acceptance Testing (UAT), system acceptance, and ongoing system updates to ensure compliance and efficiency.
  • Develop clinical supply management plans and provide input to vendor management plans, focusing on procurement, secondary manufacturing, distribution, and interactive response technology systems.
  • Participate in the selection of trial supply vendors and IRT vendors for PSI studies, ensuring alignment with business objectives.
  • Support and train PSI teams in clinical supply management, promoting knowledge sharing and best practices.
  • Liaise with PSI project teams, company divisions, clients, and vendors to ensure effective communication and collaboration.
  • Assess risks associated with clinical product management and quality incidents reported by vendors, driving proactive risk mitigation and quality improvement.
  • Support business development tasks related to clinical trial supply services, contributing to business growth and expansion.
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