Job Summary

A pharmaceutical company needs applicants for an opening for a Remote Regulatory Document Specialist.

Individual must be able to fulfill the following responsibilities:

• Complete the preparation of the Trial Master Files (TMF) for internal and external studies
• Seamlessly communicate and coordinate with our Sponsors, Project Managers, monitors and sites
• Work in clinical research and document management

Qualifications Include:

• Travel may be required
• Bachelor's degree in related field such as science, nursing, or other biomedical discipline
• Minimum 1 year document management experience
• Proficient computer skills, i.e. MS Word, Excel, PowerPoint