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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Learn more about our EEO & Accommodations request here.
Skills Required
- 5+ years of experience in clinical supply chain, clinical operations, project management, or a related pharmaceutical or 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
- Proven ability to drive operational excellence, mitigate supply risks, and ensure timely delivery of investigational products for global clinical trials
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
