Clinical Trial Documentation Specialist

Job Summary

A company is looking for a Trial Documentation Associate II.

Key Responsibilities:

• Monitor protocol and regulatory compliance of clinical research studies
• Review research data for accuracy and manage documentation and milestones
• Develop study-related documents and maintain communication with study teams regarding trial activities

Required Qualifications:

• Bachelor's degree in a relevant area required
• Minimum of 2+ years of clinical research experience in a complex disease area
• Prior experience managing clinical trial regulatory documents
• Trial Master File (TMF) experience preferred
• SOCRA or ACRP certifications strongly preferred