Job Responsibilities:
- 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.
Experience Requirements:
- Bachelor%27s degree. or higher qualification within Life Science, Pharmacology, or a relevant discipline.
- 5+ years experience in clinical or pre-clinical trial management
Skills and Competencies:
- 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 %28Word, Excel and PowerPoint%29.
Excellent English proficiency %28oral and written%29
