Under the responsibility of Project Managers (PMs) and the Clinical Operations Director, ClinSearch’s international team of experienced Clinical Research Associates (CRAs) has the ability to recruit, manage and monitor investigation sites across all of Europe, as well as some Middle Eastern and North American territories.

ClinSearch performs internal and external audits of vendors and partners for your clinical evaluations and post-marketing studies under the responsibility of our Regulatory Affairs/Quality Systems Manager. All audits are performed to assess the quality of study data and conduct and ensure compliance with the above-detailed standards.

The design of an acceptable medicine is a critical step for ensuring treatment success. Acceptability of medicine aims to prevent poor compliance and unlicensed use, especially in pediatric and geriatric populations. Over the last few years, ClinSearch has acquired valuable knowledge of predictive factors of acceptability, discovered and extracted from a large database of medicines’ evaluations.

ClinSearch is a European Health Research Organization which provides Consultancy and Operational services for Medical Device and Drug Development. Our primary geographic focus is Europe and we also provide some of our services in the Middle East and North America. We strive to offer more than quality at each step of your project, more than a highly qualified team, and more than customer satisfaction.