Description
You will head up the regulatory department and work closely with the head of clinical, as you prepare the company's innovative product for submission to the EU, FDA, and Europe. The technology is class III and the founder of the company has a track record of success with start-up companies. The location is in Palo Alto but headquarters are in Seattle, and so you can work from there as well.Looking for a candidate who has hands-on regulatory experience with cardiovascular devices and IDE's. The ideal candidate will have experience leading a regulatory team and working closely with the FDA and other international agences to get submissions passed. A passion for innovation and start-up companies is also essential.
To find out more about Real please visit www.realstaffing.com