Job Summary

A contract research organization is searching for a person to fill their position for a Telecommute Senior Medical Writer.

Core Responsibilities Include:

• Working with Project Manager to develop timelines and resource plans
• Performing quality control (QC) review
• Reviewing statistical analysis plans, summary table shells, and case report forms as required

Required Skills:

• The ability to accurately and clearly present clinical data as well as strong verbal and interpersonal communication skills
• Broad knowledge of global pharmaceutical regulatory requirements, and experience in clinical research or other areas of the pharmaceutical industry
• BS/BSc/BA in a science or industry-related discipline
• Minimum of 5 years of medical writing experience in a contract research organization (CRO), pharmaceutical, or biotech setting
• Working knowledge of ICH and other regulatory guidelines
• Proficiency in Microsoft Word and graphic presentations is required