Director, Clinical Supplies Management - ENGINEERINGUK
  • Dublin, Leinster, Ireland
  • via BeBee.com
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Job Description

**Clinical Supplies Director Role Summary:** Lead the Clinical Supplies function, providing strategic direction and ensuring timely delivery of clinical trial projects while maintaining quality and regulatory compliance.

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ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment driving innovation and excellence. **Key Responsibilities:** • Provide strategic direction and priorities for the Clinical Supplies function, executing on the strategy and adapting as required. • Ensure clinical trial projects are delivered to quality expectations in a timely manner, adhering to ICON or Sponsor SOPs, and in compliance with ethical, legal and regulatory standards. • Demonstrate oversight through regular reporting of metrics. • Drive functional activities and collaborate with Finance to manage departmental budget and achieve targeted revenue and margins. • Build customer relationships and interact with customers in a consultative, operational and business development capacity. • Build and maintain an optimal global organizational structure and allocate resources to projects and initiatives. • Establish and build effective supplier relationships and communicate company priorities and requirements. • Liaise with Procurement and Legal departments towards sourcing appropriate vendors, negotiating pricing, and structuring Master Service Agreements (MSA) and governance over vendor adherence to Service Level Agreements (SLA). • Develop, implement and maintain policies, procedures and systems related to Clinical Supplies. • Devise and drive process improvements with a focus on streamlining processes and adding value to the business. • Manage CSM quality, including resolution of clinical supplies quality issues from internally or externally driven sources. • Perform additional relevant responsibilities as directed by management. **Requirements:** • Working knowledge of regulations governing investigational products, including Good Manufacturing Practices and International Conference on Harmonization/ Good Clinical Practices guidelines. • Deep understanding of supply chain networks, clinical regulations and timelines. • In-depth experience in the pharmaceutical and/or healthcare industries in a Quality, Project Management, Logistics or Supply Chain role. • Degree level education (Biological Sciences, Supply Chain preferred). • Masters desirable **What ICON Offers:** Our success depends on the quality of our people. We've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of benefits, including various annual leave entitlements, health insurance offerings, retirement planning, and a global Employee Assistance Programme.

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