Job Summary

A major biopharmaceutical company is in need of a Remote Regulatory Writing Manager.

Individual must be able to fulfill the following responsibilities:

• Write or oversee the writing of clinical study reports and Investigator Brochures
• Prepare and oversee the preparation of regulatory submission documents
• Write CTD sections

Qualifications Include:

• Doctorate degree
• OR Master's degree and 3 years of relevant experience
• OR Bachelor's degree and 5 years of relevant experience
• OR Associates degree and 10 years of relevant experience
• OR High school diploma / GED and 12 years of relevant experience