Remote Medical Writer — Regulatory & Clinical Documentation

Placements24; Roanoke (VA); Hybrid; USD 90,000 - 130,000; Full time

Benefits offered by this job

Remote-friendly

Competitive benefits

Professional development opportunities

Job summary

Placements24 is seeking a talented Medical Writer to join its expanding medical affairs team in a fully remote capacity. You will craft scientifically accurate, regulatory-compliant documents for clinical trials, regulatory submissions, and publications, communicating complex data clearly.

The role requires 3+ years of medical writing experience in pharma/biotech/medical devices, a life sciences or English/communications background, and strong regulatory knowledge.

Qualifications

• 2–4 lines about required experience and competencies.

Responsibilities

• Write, edit, and review medical documents including CSRs, protocols, investigator brochures, and regulatory submission docs.
• Translate complex clinical data into clear, accurate content.
• Ensure documents meet regulatory standards (ICH, FDA) and company style guides.
• Collaborate with medical affairs, clinical operations, regulatory affairs, and R&D.
• Manage multiple projects and meet deadlines.
• Develop and refine document templates and writing standards.

Skills

Medical writing

Regulatory writing

Editing

Education

Bachelor's degree in life sciences/healthcare/English/communications

Job description

Placements24 is seeking a talented Medical Writer to join its expanding medical affairs team in a fully remote capacity. You will craft scientifically accurate, regulatory-compliant documents for clinical trials, regulatory submissions, and publications, communicating complex data clearly.

The role requires 3+ years of medical writing experience in pharma/biotech/medical devices, a life sciences or English/communications background, and strong regulatory knowledge.