Clinical Research Coordinator

Clinical Research Coordinator II (CRC II)

📍 New York City Area | Full-Time Hourly Benefits

We’re hiring an experienced Clinical Research Coordinator II (CRC II) to independently manage complex and high-enrolling clinical trials at a growing research site in the Boston area.

This role is ideal for a coordinator who has moved beyond entry-level responsibilities and is ready to own studies end-to-end, serve as a key sponsor-facing contact, and help drive enrollment, data quality, and inspection readiness.

What You’ll Do

• Independently manage a portfolio of complex and/or high-volume clinical trials
• Fully own study execution including screening, enrollment metrics, and visit conduct
• Conduct all participant visits, clinical procedures, and eligibility assessments per protocol
• Lead study start-up activities (SIV prep, regulatory readiness, supplies, staff training support)
• Serve as the primary liaison with sponsors, monitors, and CROs
• Oversee source documentation, data entry, and query resolution
• Maintain full investigational product (IP) accountability and compliance
• Identify operational risks and recommend corrective actions
• Compile and present study metrics to internal leadership and sponsor partners
• Train and oversee CRC Is or Research Assistants supporting your studies

What We’re Looking For

• Bachelor’s degree required
• 1 year of clinical research experience (industry-sponsored trials required)
• Demonstrated ability to manage trials independently
• Strong protocol comprehension and clinical skills
• Comfortable communicating directly with sponsors and CROs
• Highly organized, proactive, and quality-driven

Why This Role

• Clear ownership and autonomy
• Exposure to complex, sponsor-facing trials
• Growth path toward CRC III / site leadership
• Competitive hourly pay full benefits

📩 Interested or know someone great?

Apply directly on LinkedIn or message me to discuss details confidentially.