Qualification/background
MD with Board certification in oncology with direct or indirect exposure in clinical development (not neccesary. Responsibility/key activities
Medical leadership and expertise in clinical trials, input into clinical trial design, design/review/sign off of Protocol, IB, CRF, ICF, Study Manual, IMPD, medical writing (clinical study report), medical review of data, publication plan, medical/clinical review of regulatory submissions (clinical/medical part), oncology medical training and education, ensure clinical trial quality and consistency (study/protocol queries, deviations, protocol amendments), Advisory Boards, Investigators´ Meetings, Review of SAE
Skills/knowledge/competencies
Fluent Czech, English – spoken and written (+ writing skills), presentation skills, ability and willingness to , willingness to travel (Europe, US), communication and interpersonal skills, time management, result oriented, ICT (MS Office, IN)
Region:Czech Republic, Europe, USA
In case of interest please send your CV to Marcela Bukačová at bukacova@hays.cz
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