To assure the implementation of project plans as assigned, Ethics committee and competent authority regulatory submissions of clinical trials applications, site monitoring & site management responsibility according to ICH Guidelines and GCP, local regulations, study requirements and SOPs.
University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution
In lieu of the above requirement, candidates with with experience as CTA or Study Coordinator will be considered
Fluent in local office language and in English, both written and verbal
Excellent interpersonal relationships and team player
Energetic, Effective, Assertive and well motivated
Excellent planning and organization skills
Work under pressure and independently
Excellent computer skills including: Outlook, Word, Excel, PowerPoint
Work is Sunday-Thursday 8:00-17:00.
Location in the area of Modiin.
Send your CV via email only: info@Q-Trials.com.
Only relevant applications will be answered.