Support for study patients and takeover of assistance activities according to the respective study protocols (phase I-IV) incl. Collection and documentation of all study-relevant data in the files and CRFs Organization and coordination of business and diagnostics, if necessary acceptance and preparation of laboratory samples including Shipping Proper storage and protocol-compliant output of the test medication – under supervision of the respective test physician/test physician Preparation, monitoring and follow-up of monitor visits, audits and government inspections Organization of correspondence with the study management

Complete training in a medical profession or comparable professional experience Continuing and continuing training for the student assistant or willingness to complete these Multiannual experience in carrying out international clinical trials of Phase II-IV is desirable Good English knowledge of word and writing, MS Office and database Knowledge of GCP is desired This position also requires a high degree of thorough and independent work, very good communication skills, a pronounced coordination and organisational ensemble as well as great resilience.

A varied, versatile and demanding task area in a young, collegial team 38.5 weekly hours A qualified incorporation concept Internal continuing and continuing training Price options All benefits customary in the public service, e.g. supplementary pension Daycare centre Personnel accommodation Remuneration is effected according to TV-L in the pay group 9a, with the calculation of all previous times in accordance with the tariff regulations. Disabled applicants are preferably taken into account with the same suitability. Parttime employment is possible. .