Fortrea

Clinical Supply Project Manager, Sponsor-Dedicated (FSP)

In short

This hybrid Istanbul role manages and coordinates clinical supply activities, ensuring efficient distribution of investigational products and ancillary materials across clinical studies. Fortrea is a CRO hiring for a sponsor-dedicated team in Türkiye, working with sponsors, depots, vendors, packaging organizations, and cross-functional study teams. It requires 5+ years of experience in Clinical Supply Chain, Clinical Operations, or Project Management in a pharmaceutical/CRO environment, with strong end-to-end supply process knowledge.

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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