Remote Nonclinical Regulatory Writer — Lead Submissions

A clinical research organization is seeking a Regulatory Writer to manage and develop technical nonclinical documents. This full-time, remote position requires at least 2 years of writing experience in the pharmaceutical industry, strong analytical skills, and proficiency in MS Office. Ideal candidates will have a bachelor's degree in a relevant field and knowledge of GLP and ICH guidelines. Join a supportive team dedicated to shaping the future of clinical research. #J-18808-Ljbffr