Clinical Trial Support Center

Atsushi HASHIZUME
Director,
Professor

The Clinical Trial Support Center serves as a specialized unit dedicated to supporting the conduct of clinical trials and clinical studies. We are committed to promoting high-quality clinical research while placing the highest priority on the safety, rights, and well-being of research participants.
In recent years, the development of pharmaceuticals and medical devices has undergone significant transformation. Advances in study design, the integration of digital technologies, and the increasing complexity of clinical research have reshaped the way clinical trials are conducted. In this evolving environment, the Clinical Trial Support Center is expected not only to facilitate the efficient operation of studies but also to ensure both scientific integrity and the protection of research participants.
At our center, Clinical Research Coordinators (CRCs) and other specialized staff work closely with principal investigators and relevant departments to support participant engagement, study operations, and a wide range of coordination activities essential to the successful conduct of clinical research.
We strive to provide an environment in which individuals can participate in research with confidence and peace of mind, while continuously supporting high-quality clinical research that contributes to advances in healthcare and medicine. We sincerely appreciate your understanding and cooperation and look forward to your continued support.

The Clinical Trial Support Center provides operational support for the on-site conduct of clinical trials and studies. Clinical research coordinators (CRCs) and other specialized staff support participant management and trial operations, ensuring that studies are conducted appropriately and efficiently. The Center also establishes the operational infrastructure necessary to support trials, including investigational product management and coordination with relevant departments. In collaboration with the Clinical Development Center and the Data Center, it contributes to the high-quality conduct of clinical trials and the protection of participant safety.