Why choose us
Each clinical project is managed by a specifically assigned Study Coordinator in order to ensure that the highest industry expectations are fulfilled. Study Coordinators cooperate closely with the medical department head and the Principal Investigator. They are responsible for smooth and appropriate conduct of their clinical research project within established timelines, protocol requirements, contractual limitations and quality standards.
Study Coordinators are responsible for the administrative part of the studies. They report study status to the sponsors, maintain daily contacts with monitors, subcontractors (e.g. laboratories),
IEC/IRB and regulatory authorities. They supervise the completeness and quality of the source documentation and CRFs, as well as keep the Site Master File up to date.