Jobtailor in New Jersey is seeking an experienced regulatory professional to coordinate global submissions and support agency meetings. You will work with subject matter experts to prepare high-quality regulatory documents and respond to agency queries.
Candidates should have an MD/PhD/PharmD and 2+ years regulatory experience, with strong US FDA knowledge, attention to detail and excellent written and verbal communication.
#J-18808-LjbffrOncology Regulatory Strategy Lead — Global Submissions in nj at Unknown Company
This position is listed as full time and onsite.