Senior CRA II Sponsor dedicated based in Türkiye
On-siteIstanbul, Istanbul, Turkey
Job Summary
Act as primary contact for assigned clinical trial sites, managing the full lifecycle from start-up through monitoring and close-out while ensuring delivery to timelines and quality standards. Conduct on-site and remote monitoring to identify risks and drive timely issue resolution, ensuring compliance with study protocol, ICH-GCP, and local regulatory requirements. Oversee site performance including data quality, recruitment, training, and documentation completeness, and collaborate cross-functionally to implement site strategies and support feasibility, activation, and audit readiness. This sponsor-dedicated role within Fortrea's Türkiye office offers strong autonomy and direct collaboration with a leading global biopharmaceutical partner to advance cutting-edge therapies.
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
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