Job Summary

A clinical research organization is in need of a Remote Senior Regulatory Medical Writer in King of Prussia.

Core Responsibilities Include:

• Evaluating, analyzing, and interpreting medical literature to select resource materials
• Writing and editing clinical development documents
• Mentoring medical writers and other writing members of the project team

Applicants must meet the following qualifications:

• At least 3 years of previous experience in the pharmaceutical industry
• 3-5 years of industry regulatory writing and clinical medical writing experience
• Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
• Experience being a project lead or managing a project team
• Exceptional writing skills
• Understanding of clinical data