Senior Medical Writer: Regulatory Submissions Expert
Listed on 2026-10-06
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Pharmaceutical
Medical Science Liaison -
Healthcare
Medical Science Liaison
MMS is a Denver-based, data-focused CRO providing regulatory submission support for pharma, biotech and medical device trials. The Medical Writer will interpret literature, prepare regulatory documents and manage writing projects in a fast-paced environment.
Ideal candidates have 3+ years in pharmaceutical regulatory writing, strong MS Word/PowerPoint skills, and experience leading teams under tight timelines. Strong communication and knowledge of ICH guidelines are a plus.
This is an excellent opportunity to take on the Senior Medical Writer:
Regulatory Submissions Expert role at MMS.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Denver, CO, United States.
This opportunity is part of our work in Marketing & Media, Bio & Pharmacology & Health.
The advertised compensation is 90..
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