All studies contracted with CRS-Group members are organised by study teams. The organisation of the trial as well as the coordination of the communication between Sponsor, internal departments and our external partners is the primary function of the Project Management/Coordination.

It is ensured that only few persons will be the main contact partners for the Sponsor during the clinical conduct of the trial. The Project Management/Coordination is responsible for time and logistic planning, preparation of submissions to the Ethics Committee and relevant authorities, management of the trial and keeping the communication process.