Senior Nonclinical Writer — Remote, Lead Submissions
Charlotte, Mecklenburg County, North Carolina, 28245, USA
Listed on 2026-10-02
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Research/Development
Regulatory Compliance Specialist
MMS is a data-focused CRO helping pharmaceutical, biotech, and medical device industries with trial data and regulatory submissions. This remote, full-time role focuses on nonclinical regulatory writing and management of complex documentation for INDs, CTAs, NDAs, BLAs, and MAAs.
You will lead writing efforts based on GLP/non-GLP data, collaborate with cross-functional teams, and ensure scientific integrity and regulatory compliance across modules 2.4 and 2.6 of eCTD submissions.
As a Senior Nonclinical Writer — Remote, Lead Submissions, you will play an important part at MMS in United States.
This role, Senior Nonclinical Writer — Remote, Lead Submissions at MMS, could be your next opportunity.
Are you ready to take on the Senior Nonclinical Writer — Remote, Lead Submissions role at MMS?
We would love to welcome a new Senior Nonclinical Writer — Remote, Lead Submissions to our organisation in United States.
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