Remote Regulatory Affairs Consultant - Orphan Drug

A leading consultancy firm is seeking a Regulatory Affairs Consultant for remote support on regulatory submission programs. The role requires approximately 10 hours per week, focusing on FDA communications and regulatory documentation through Lorenz docuBridge TWO. Candidates should hold an advanced degree in science or biomedical engineering and have at least 4 years of experience in filing global regulatory applications. This position offers flexibility in a professional and inclusive environment. #J-18808-Ljbffr