Field Clinical Research Associate III

📋 Description

• Serve as site manager; ensure data entry, query resolution, audit readiness.
• Monitor study activities: site management, initiation, monitoring, closeout.
• Monitor compliance with study protocols and regulatory guidelines.
• Prepare study conduct requirements and train sites.
• Manage device accountability, inventory, and distribution; track issues.
• Draft regulatory documents; CRFs, protocols, manuals; mentor staff.

🎯 Requirements

• Bachelor’s degree in Biological sciences/health field; 5+ yrs clinical research; 2+ yrs monitoring.
• Strong knowledge of medical terminology.
• Knowledge of laws/regulations governing clinical studies.
• Excellent verbal, written, and interpersonal communication.
• 40-60% travel; strong organizational and problem-solving skills.
• MS Office proficiency; ability to mentor junior staff.

🎁 Benefits

• Collaborative team with constant learning.
• Part of a team advancing treatments for serious diseases.
• Generous benefits: medical, dental, vision, life, AD&D, disability.
• 401(k) with employer match; paid parental leave.
• Eleven company holidays and at least 15 vacation days.
• Paid sick time per applicable law.