Fortrea

Senior CRA II Sponsor dedicated based in Türkiye

Türkiye · Remote (restrictions not stated) · Full time

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About the role

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EmployerFortrea
LocationTürkiye
Work styleRemote (restrictions not stated)
Employment typeFull time
Employer posted15 Jul 2026

Join Fortrea as a Senior Clinical Research Associate II in Türkiye within a sponsor-dedicated model, where you will work exclusively with a leading global biopharmaceutical partner.

In this role, you will support the delivery of high-quality clinical trials across innovative therapies, building strong site relationships and ensuring excellence in study execution.

Working in this model offers close collaboration with the sponsor’s teams, strong study ownership, and the opportunity to contribute directly to advancing cutting-edge treatments for patients worldwide.

Core responsibilities:

Act as primary contact for assigned clinical trial sites, building strong, collaborative relationships
Manage site lifecycle from start-up through monitoring and close-out, ensuring delivery to timelines and quality standards
Conduct on-site and remote monitoring, identifying risks and driving timely issue resolution
Ensure compliance with study protocol, ICH-GCP, and local regulatory requirements
Oversee site performance including data quality, recruitment, training, and documentation completeness
Support study execution (e.g. feasibility, site activation, investigator meetings, audit readiness)
Collaborate cross-functionally to implement site strategies and ensure successful trial delivery

Show full description

Required Qualifications:

Bachelor’s degree in Life Sciences or equivalent experience
≥5 years’ experience in clinical research, including site monitoring/site management
Proven experience in Oncology, Ophthalmology, Gene Therapy or similar therapeutic area
Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
Solid problem-solving and critical thinking skills
Proficiency in Turkish and in English
Willingness to travel

Join Fortrea and take ownership of clinical trial sites across innovative therapies, playing a critical role in delivering high-quality data and accelerating drug development. This role offers strong autonomy, cross-functional collaboration, and exposure to cutting-edge clinical research.

If you are passionate about advancing clinical research and want to grow your expertise in a sponsor-dedicated environment, we encourage you to apply and join us in making a meaningful impact on patients’

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