Overseeing multi-center studies in Israel, Europe, and the US.
Participate in pre-clinical and clinical study design, including selection of study sites and vendors.
Accountable for the studies budget, quality, deliverables and timelines.
Participate in protocol development and CRF design.
Planning, implementation and tracking of the clinical monitoring process and maintaining an overview of ongoing clinical trials.
Proactively identify and resolve studies risks.
Requirements: Bachelor's degree / higher qualification within Life Science, Pharmacology, or a relevant discipline
5+ years experience in clinical or pre-clinical trial management
Excellent organizational and planning skills.
Strong communication skills.
Detail oriented, with an ability to multitask and prioritize in a fast-paced environment.
Good problem-solving abilities, flexibility, team player with excellent interpersonal and presentation
skills.
Proficient use of standard MS Office applications (Word, Excel and PowerPoint).
Excellent English proficiency (oral and written)
המשרה מיועדת לנשים ולגברים כאחד.