Senior Medical Writer: Regulatory Submissions Expert
Listed on 2026-11-05
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Pharmaceutical
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Research/Development
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.
The Senior Medical Writer:
Regulatory Submissions Expert position in the Marketing & Media, Bio & Pharmacology & Health field is open for applications.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Medical Writer:
Regulatory Submissions Expert role in the description above.
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