Senior Nonclinical Regulatory Writer for DMPK/BA Submissions

An established industry player is seeking a Nonclinical Regulatory Document and Scientific Writer to join their dynamic team. This role requires a strong background in DMPK and regulatory drug development, with responsibilities including authoring and reviewing critical regulatory documents for various therapeutic areas. The ideal candidate will possess exceptional analytical skills and project management capabilities, ensuring the timely completion of documentation while collaborating with subject matter experts. Join a forward-thinking company where your contributions will directly impact drug development programs across global markets, and thrive in an environment that values initiative and accountability. #J-18808-Ljbffr