Senior Regulatory Writer – Clinical Submissions Lead

A global biopharmaceutical organization is seeking a Senior Regulatory Writer to lead and participate in project teams focused on regulatory documentation. Candidates should have at least 3 years of regulatory writing experience and a Bachelor\’s degree. This role involves authoring documents per client specifications and regulatory guidelines, managing project budgets, and coaching junior staff. The ideal candidate will demonstrate strong Microsoft Word proficiency and an understanding of the drug development lifecycle. Competitive salary and opportunities for professional growth are offered. #J-18808-Ljbffr