This role blends traditional clinical project management with the operational coordination of digital tools, platforms and IT services used in patient-centric studies. * Serve as the primary point of contact for the sponsor and drive project planning, execution and timelines - from study-start activities through ongoing study management to the coordination of all phases of the clinical-trial lifecycle. * Our contract offer: a fair compensation package, permanent employment, 30 vacation days on a 5-day week, flexible working hours, overtime compensation and the option to work up to three days per week (60:40 model) from home or, depending on location, fully remote.
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