Description
I am currently working with a client who is beginning a search for a Senior Vice President of Regulatory & Clinical Affairs. The company is currently based in Dallas, TX but is strongly considering a move to Orange County.My client is a Class III medical device start-up focusing in Ophthalmic therapies. They are currently under way with early stage clinical trials for their innovative device. The ideal person for this position is someone with strength in regulatory and clinical strategy, interfacing with global regulatory agencies and expertise with the FDA. As this is a C-level position, this person will play a major role in guiding the future direction of the company. The individual need not have been a VP before as long as s/he meets the qualifications.
Qualifications:
An ideal candidate will be someone who is creative and can provide options when it comes to regulatory pathways and seeking the best way to approval. Because the company is a start-up, it will be a very hands-on position. This person must have:
- PMA submissions experience
- Experience designing multi-site clinical trials
- Ophthalmic experience is preferred but not necessary
- A passion for and successful track record with start-up companies and innovation
To find out more about Real please visit www.realstaffing.com