Medical Devices company are looking for Clinical Studies Manager.
Lead all preparations for clinical trials (study design, protocols, sites, CRF, ICF, IRB).
Responsible for sites management (contracts, initiations, monitoring, follow ups, closure) and summary of clinical work.
2- data analysis, reports, white papers, publications (secondary).
Collaboration with Regulatory affairs.
Degree in biologic/biomedicine/Statistics.
At least 3 year experience in the same position and tasks.
Experience in medical device company-highly recommended.
English high level.
המשרה מיועדת לנשים וגברים כאחד.