Contact person for medical staff, patients, sponsors, and monitors, Planning and coordination of clinical studies, including organization of diagnostics and laboratory and sample shipping or storage, Preparation and support of initiations, monitor visits, audits, and inspections, including follow-up, Creation and maintenance of study-relevant databases, as well as documentation and archiving of study data (e.g., eCRF, MS Access), Implementation of study-relevant requirements according to GCP/ICH, as well as performance of administrative tasks, correspondence, and preparation of internal study meetings