Senior Medical Writer – Regulatory Submissions & Study Lead
Listed on 2026-09-29
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Research/Development
Clinical Research, Medical Science, Regulatory Compliance Specialist
MMS Holdings Inc is seeking a Medical Writer to evaluate literature, design studies, and prepare regulatory documents for clinical development. You will author or co-author protocols, reports, consent forms, and safety summaries, while meeting tight timelines and maintaining document quality.
The ideal candidate has 3+ years in pharmaceutical regulatory writing and strong leadership skills, with advanced MS Word, Excel, and PowerPoint proficiency.
This is an excellent opening to take on the Senior Medical Writer – Regulatory Submissions & Study Lead role at MMS Holdings Inc.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Medical Writer – Regulatory Submissions & Study Lead role in the description above.
We appreciate your interest in this position.
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