Lead Regulatory Writing & Submissions Strategy

A leading biopharmaceutical company seeks an Associate Principal Regulatory Writer in Upton, Pennsylvania. You will contribute to regulatory submissions, leading project teams and mentoring junior writers. This role requires extensive regulatory writing experience and a strong understanding of the drug development process. The ideal candidate has a Bachelor's degree, with MS or PhD preferred, and over 8 years of relevant experience, ensuring high-quality documentation aligned with regulatory standards. #J-18808-Ljbffr