Senior Nonclinical Regulatory Writer — Remote UK

MMS Holdings Inc. in the United Kingdom seeks an experienced regulatory writer to develop and manage highly technical nonclinical documents for regulatory submissions.

You will lead projects independently and collaborate with cross-functional teams to ensure documentation meets current guidelines. You will work on modules 2.4/2.6, IBs, and nonclinical study reports, with emphasis on GLP and ICH considerations.

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