You support the distribution and tracking of critical clinical documents and information, e.g. essential documents, study supplies, budgets, manuals, other site and subject related information and investigational product releases in collaboration with the study team. * Your proficiency in MS Office and electronic clinical trial data management systems, e.g. CTMS or eTMF, is expected. * 30 days of vacation, discounted ticket to Germany, (e)-bike leasing, capital-forming benefits, company pension plan, disability insurance, canteen, and much more.
mehr