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

Fortrea; Fatih; Hybrid; TRY 600,000 - 900,000; Full time

Job summary

Fortrea is expanding its sponsor-dedicated team in Türkiye and seeks an experienced Clinical Supply Project Manager based in Istanbul. This hybrid role will support the distribution of investigational products across multiple studies while ensuring regulatory compliance and effective supply planning.

The candidate will work with sponsors, depots, vendors, and cross-functional study teams to mitigate risks and drive execution of global supply strategies, with a focus on timely delivery and

Qualifications

• 5+ years of experience in Clinical Supply Chain, Clinical Operations, Project Management, or related pharmaceutical/CRO environment.

Responsibilities

• Manage and coordinate clinical supply activities to ensure efficient distribution of investigational products and ancillary materials across clinical studies.
• Collaborate with sponsors, depots, vendors, packaging organizations, and cross-functional study teams to drive supply planning and timely delivery.

Skills

Clinical supply

Forecasting

Vendor collaboration

Project management

Regulatory compliance

Job 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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