Dedicated Study Coordinators serve as an extension of the investigative site team, ensuring seamless execution of day-to-day study activities. From visit scheduling and source documentation management to EDC support and patient follow-up, our coordinators help maintain compliance, efficiency, and data quality throughout the study.

Our regulatory specialists provide end-to-end support for ethics committee and competent authority submissions, amendments, safety notifications, and essential document management, ensuring full regulatory compliance at every stage of the study.

Accurate site selection is key to study success. Orjin CRS conducts comprehensive feasibility assessments by evaluating patient availability, site capabilities, investigator experience, competing studies, and recruitment potential, helping sponsors identify high-performing research sites across Türkiye.

We streamline site activation by coordinating all critical start-up activities, including document collection, feasibility follow-up, contract support, training coordination, and regulatory submissions. Our structured approach minimizes start-up timelines and enables sites to initiate recruitment efficiently.

We provide tailored operational support to investigators and site teams, enabling them to focus on clinical and scientific responsibilities. Our services include study planning, training coordination, communication management, documentation oversight, and operational troubleshooting to maximize site productivity and compliance.

Patient recruitment remains one of the most critical factors influencing study timelines. Through site-specific recruitment strategies, patient pathway analysis, referral network engagement, and recruitment performance monitoring, we help sites achieve enrollment targets efficiently while maintaining patient-centricity and retention.