Lead Remote Nonclinical Regulatory Writer
MMS
Boston, MA
- Remote job
MMS is a data-focused clinical research organization renowned for its culture and global reach. This full-time remote role focuses on development, writing, and management of highly technical nonclinical documents, including Module 2.4/2.6 eCTD submission components and IBs. You will lead writing projects, interpret GLP/nonclinical data, map placements in eCTD, and ensure alignment with regulatory guidelines while collaborating with cross-functional teams across project management, safety, and #J-18808-Ljbffr MMS
Vacancy posted 3 days ago
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