Job Description
The main task of the CRA is to act as a link between sponsor, CRO and trial site as well as to perform quality control of clinical trials. The focus is on clinical studies conducted in-house at bioskin or in the Northern German region.
Your main responsibilities:
Perform all kind of the monitoring visits (site selection, initiation, periodic and close-out visits) as well as remote monitoringGeneration and updating of monitoring plans and site initiation presentationEvaluating the quality and integrity of site practicesAct as contact for clinical trial suppliers and other vendors as assignedIdentifying and escalating protocol deviations, discrepancies in data, and non-compliance to clinical trial protocolsClose cooperation with the different departments in-house at bioskin as well as freelance CRAsCompliance with protocol, GCP/ICH GuidelinesQualifications