Clinical Research Operations Specialist II

Job Summary

Providing live support and managing multi-site operations, the full-time Clinical Research Operations Specialist II will oversee participant recruitment, data management, and compliance for a large cardiovascular clinical trial in a remote setting.

Key responsibilities

• Oversee subject recruitment and study enrollment goals, implementing effective strategies for participant retention
• Manage data collection and reporting systems, ensuring compliance with regulatory standards
• Collaborate with principal investigators and study sponsors to monitor adverse events and resolve study queries

Required qualifications

• Bachelor's degree in a related field with two years of clinical research experience or equivalent education and experience
• Proficiency in Microsoft Office and database applications
• Knowledge of research protocols and regulatory requirements, including HIPAA and FDA regulations
• Experience with medical terminology
• Certification from the Society of Clinical Research Associates or Association of Clinical Research Professionals is preferred