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
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’
#LI-CB1 #LI-Remote
Learn more about our EEO & Accommodations request here.
Skills Required
- Bachelor's degree in Life Sciences or equivalent experience
- 5+ years' experience in clinical research including site monitoring/site management
- Proven therapeutic area experience in Oncology, Ophthalmology, Gene Therapy or similar
- Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
- Proficiency in Turkish and English
- Willingness to travel
- Experience supporting study execution (feasibility, site activation, investigator meetings, audit readiness)
- Strong problem-solving and critical thinking skills
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.
