Clinical Research Associate

Job Summary

A company is looking for a Clinical Research Associate (CRA).

Key Responsibilities

• Assist with study planning, execution, and investigator site management
• Write and assemble regulatory submissions, draft study protocols and reports
• Monitor investigational sites for protocol adherence and oversee patient enrollment

Required Qualifications

• 5+ years of clinical research monitoring experience
• Bachelor's degree in Life Sciences
• Strong knowledge of ICH GCP, FDA, and IRB requirements
• Experience in independent site monitoring and management
• Leadership experience, including mentoring junior CRAs