Senior Nonclinical Writer — Lead Submissions (Remote)

MMS is seeking a regulatory nonclinical writer for a full-time remote role based in the UK. You will develop and manage highly technical nonclinical documents for regulatory submissions, ensuring scientific integrity and compliance with GLP, ICH, FDA and EMA guidelines.

Ideal candidates have 5+ years in regulatory nonclinical writing, strong MS Office skills, and proven ability to lead complex projects across cross-functional teams within a CRO environment.

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