Study Coordination
We offer comprehensive on-site study management, including the recruitment and instruction of study participants and/or patients as well as planning, preparation and conducting of participant's study visits.
We collect study-specific data on preferably on electronic case report forms and collect, prepare, store and ship study samples according to the protocol. We also prepare quality management relevant documents for quality management and plan and execute logistical procedures such as ordering consumables.
Our qualified study coordinators act as point of contact for your patients, healthy participants or monitors. They offer you diverse support in the daily clinical study routine and carry out various tasks. By creating activity plans and communicating internally with stakeholders, we ensure that the study coordinators involved are up to date during your study. Special care is taken to ensure compliance with GCP guidelines, legal requirements, standardized processes and, of course, protocol requirements.
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