Clinical Development Medical Writer

Shape clinical development documents at MMS through rigorous literature analysis, regulatory writing, and interpretation of clinical data. Work with clients and multidisciplinary project teams.

This Principal Medical Writer authors and edits documents supporting clinical research and regulatory submissions. Assignments include protocols, investigator brochures, clinical study reports, consent forms, safety and efficacy summaries, and Module 2 documents. You will also prepare presentations and medical journal publications.

• Analyze primary literature for study design and scientific rigor
• Author clinical protocols as well as development documents
• Produce interpretive guides and publication materials
• Manage writing workflows and complete assignments promptly
• Consult project teams and mentor writers as needed

• Bachelor’s, master’s, or PhD scientific degree
• Six years of previous regulatory writing experience
• Substantial protocol experience as lead author
• Exceptional writing and organizational skills
• Understanding of federal regulations, Good Clinical Practices, and ICH guidelines

Use clinical development expertise, precise writing, and project coordination to deliver evidence-based documents for MMS clients.