Clinical Research Coordinator

Clinical Research Coordinator II (CRC II)

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.

• 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

• 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

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

Mid‑Senior level

Full-time

Research

Research Services;
Hospitals and Health Care

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