Senior Regulatory Medical Writer & Project Lead
Listed on 2026-09-17
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Pharmaceutical
MMS is a data-driven CRO supporting the pharmaceutical, biotech, and medical device sectors. We seek a Medical Writer with 3+ years in regulatory and clinical writing to develop protocols, reports, and submission documents.
You will work with global clients, manage writing timelines, and mentor junior writers while ensuring regulatory standards and quality. This role emphasizes collaboration, scientific rigor, and timely delivery.
Join us at MMS as our next Senior Regulatory Medical Writer & Project Lead in United States.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Senior Regulatory Medical Writer & Project Lead role at MMS, based in United States.
We are looking to fill the Senior Regulatory Medical Writer & Project Lead position at MMS in United States.
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