Clinical Research Coordinator

Description

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.

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

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

Requirements

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.

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

Benefits

• Fully own study execution including screening, enrollment metrics, and visit conduct
• Growth path toward CRC III / site leadership
• Clear ownership and autonomy
• Exposure to complex, sponsor-facing trials
• Competitive hourly pay + full benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance