Job Summary

A non-profit research organization is filling a position for a Remote Regulatory Publishing Specialist.

Core Responsibilities Include:

• Supporting Regulatory Affairs in the planning, development, and publishing of submissions
• Ensuring tracking and archiving of regulatory documentation lifecycle
• Supporting drafting and review of regulatory documentation for clinical and nonclinical studies

Position Requirements Include:

• Occasional travel may be required
• 1-2 years of experience with, and knowledge of, electronic common technical document submission processes
• 2-3 years of relevant experience in clinical trials
• The ability to understand requirements in whole and in detail and the ability to effectively perform analysis
• Excellent written and verbal communication skills
• A willingness to stay abreast of new developments in the area of professional competence