Join our team! We are seeking a regulatory affairs professional with 10-15 years of demonstrated experience in pharmaceutical development, including domestic and European filings. This position requires a scientific degree and a strong understanding of the drug development process, with an emphasis on CMC DS/DP development. A willingness to provide leadership and guidance to our client's scientific team, and the ability to assist the regulatory group in preparing for their Pre-IND meeting and ultimate IND filing is a must.
No phone calls, please.