Senior Medical Writer – Regulatory Submissions & Study Lead
Listed on 2026-10-20
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Pharmaceutical
Regulatory Compliance Specialist, Medical Science Liaison
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.
Our organisation is growing, and we are hiring a Senior Medical Writer – Regulatory Submissions & Study Lead in New York, NY, United States.
We are seeking a motivated Senior Medical Writer – Regulatory Submissions & Study Lead to join MMS Holdings Inc in New York, NY, United States.
Consider building your career as a Senior Medical Writer – Regulatory Submissions & Study Lead at MMS Holdings Inc.
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