VP Clinical Affairs

Responsibilities

The VP of clinical affairs will be responsible for the design of the clinical studies together with our SAB. The VP will plan the logistics and submit the regulatory files for the FDA and IRBs. The VP will also be responsible for the trial and execution in the US, Israel and Europe. The VP will then be responsible for the analysis of the results, monitoring and submissions.

Qualifications

at least 7 years experience in clinical studies and at least 1 job as VP/director of clinical affairs in a medical device company.

Ability to travel abroad in the next 12 months at a rate of a 6 days every 2-3 months

Preferably PhD but in any case relevant education

Excellent personal conduct with all types of clinical staff