As the leading Site Management Organization (SMO) in Bulgaria, we bridge pharmaceutical companies, CROs, hospitals, patients, principal investigators, and authorities to ensure smooth and efficient administration of clinical trials.
We collaborate with the leading university hospitals in Bulgaria, giving us access to a network of key opinion leaders (KOLs) and top-tier clinical sites. Our expertise spans multi-centric clinical trials across various therapeutic areas, allowing us to manage every phase of clinical research with precision.
By centralizing processes and maintaining close partnerships with sponsors, CROs, and investigators, CLINÉCA ensures faster trial completion, improved data quality, and seamless workflows – so you can focus on groundbreaking results without the administrative burden.
Whether you’re looking for feasibility management, project start-up support, or complete trial administration, our team provides the solutions to streamline your clinical research from start to finish.
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Services
Expert site management services for local and global CROs and pharma companies
Feasibility Management
Feasibility requests are centrally managed by a dedicated feasibility manager, supported by the most experienced investigators in each field.
Project Startp-Up
CLINÉCA maintains a comprehensive database for start-up documents, enabling our research coordinators to swiftly prepare and submit the necessary paperwork, significantly shortening study start-up timelines.
Contract Management
Contracts are managed centrally by a single point of contact, ensuring standardization, efficiency, and significantly shorter start-up timelines.
Recruiting Support & Concept Development
Our network of referring physicians covers a substantial part of Bulgaria, providing access to a vast patient population, ensuring fast and reliable recruitment, even for rare indications.
Project Management
CLINÉCA’s project managers anticipate and manage risks throughout the clinical trial process, overseeing every aspect from site feasibility and communication to supply handling, study follow-up, and final database lock. This proactive approach ensures successful outcomes and smooth operations at every stage.
Quality Management
To maintain the highest standards, CLINÉCA permanently monitors and centrally manages all operational processes via our advanced CTMS system, guaranteeing consistency and quality across all network sites. Our dedicated QA department regularly performs on-site audits and quality visits, aiming to ensure the ultimate quality of data delivered.
Board of Directors
We are seasoned professionals with deep and extensive expertise in clinical research
Dr. Hristiyan Kosturski is well resourced, experienced, and together with his team is able to offer unmatched services, ensuring a smooth and efficient course of all clinical research processes.
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Hristiyan Kosturski
CEO
