Research Protocol Associate

Job Summary

A company is looking for a Research Protocol Associate.

Key Responsibilities

• Assist with clinical trial development, implementation, and maintenance
• Gather regulatory documents and draft informed consent forms
• Coordinate study logistics, approvals, and protocol modifications

Required Qualifications

• Bachelor's degree or associate degree with 2 years of relevant experience
• Proficient in Microsoft applications and research systems
• Experience with regulatory documents and IRB submissions preferred
• Experience in clinical trials or data management is helpful
• Must be a U.S. citizen, permanent resident, refugee, or asylee