Clinical Research Associate

A unique CRO company in its field in the center area in Israel, is looking to hire a CRA for an interesting and challenging position. Preferably a former contract research coordinator with at least one year of experience in the field of clinical studies with immediate availability for work. In addition to monitoring clinical trials throughout the country, the position includes responsibility for all the different aspects of the research, submissions to the Helsinki Committees and the Ministry of Health, assistance in protocol and CRF design, training involved medical centers, clinical database maintenance. Responsible for all study reports, and research aids. Coordination of activities and working with external parties involved in the study: pharmacy, laboratories, data analysis, etc. The position reports

directly to the CEO of the company. 

:Required Skills

BA or MSc in the field of life sciences or biomedical field- mandatory

GCP and CRA course is mandatory

Experience in submissions to the Helsinki Committees and the MOH

Familiarity with "Matarot" software

Familiarity with EDC systems for data collection.

Experience in writing supporting documents for clinical research

Excellent communication and written skills

English language speaking at a good level

Driver's license mandatory

The position is a position of trust that requires the ability to work independently and take responsibility. Organizational ability, paying attention to the small details, orderliness at work, punctuality, reliability, ability to deal with stressful situations, ability to learn details and a lot of information in a short time, excellent human relations. The position is a full-time work, from the office, in the medical centers with the possibility of work from home (hybrid model).