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Fortrea

Clinical Supply Project Manager, Sponsor-Dedicated (FSP), Türkiye

Fortrea Istanbul, Istanbul, Turkey

Biotechnology Research · 10,001+ employees

Nov 03
project-manager Senior (5-10 yrs) Full-time Turkey
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About the role

The Clinical Supply Project Manager coordinates clinical supply activities to ensure the efficient distribution of investigational products and ancillary materials. They work with internal stakeholders and vendors to ensure regulatory compliance and the successful execution of global supply strategies.

What they look for

Clinical Supply Chain Clinical Operations Project Management Supply Planning Inventory Management Regulatory Compliance Forecasting Packaging Distribution Import/Export Risk Mitigation Stakeholder Management Vendor Management Operational Excellence

Requirements

Candidates must have 5+ years of experience in clinical supply chain, clinical operations, or project management within a pharmaceutical or CRO environment. A strong understanding of end-to-end clinical supply processes and the ability to manage complex, cross-functional projects is required.

Full description

We are currently expanding our sponsor-dedicated team in Türkiye and are looking for experienced Clinical Supply Project Managers.

This hybrid position is based in Istanbul.

While this role is for anticipated future opportunities in Türkiye, we would be delighted to engage with talented professionals who would like to be considered for upcoming openings.

The Clinical Supply Project Manager is responsible for managing and coordinating clinical supply activities to ensure the efficient distribution of investigational products and ancillary materials across clinical studies. Working closely with internal stakeholders, vendors, and study teams, the role ensures compliance with regulatory requirements, effective supply planning, and the successful execution of global supply strategies.

Requirements:

  • 5+ years of experience in Clinical Supply Chain, Clinical Operations, Project Management, or a related pharmaceutical/CRO environment.
  • Strong understanding of end-to-end clinical supply processes, including forecasting, packaging, distribution, import/export activities, and inventory management.
  • Experience collaborating with sponsors, depots, vendors, packaging organizations, and cross-functional study teams.
  • Excellent organizational and project management skills with the ability to manage competing priorities in a fast-paced environment.
  • Proven ability to drive operational excellence, mitigate supply risks, and ensure timely delivery of investigational products to support global clinical trials.

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