Clinical Research Coordinator

Our client, a healthcare research company, is seeking a Clinical Research Coordinator to support the daily operations of active clinical trials at its Boston site. The role works directly with principal investigators, study sponsors, and enrolled participants to keep studies running in line with protocol and regulatory requirements.

The coordinator manages participant screening, enrollment, and follow-up visits, and maintains accurate study records. This position also handles regulatory documentation, data entry, and communication with sponsors and institutional review boards.

This is an on-site, full-time position suited to a candidate with prior clinical research experience who is organized, detail-oriented, and comfortable working in a regulated environment.

Responsibilities

• Screen, recruit, and enroll eligible participants according to study protocols
• Schedule and conduct study visits, including collecting vital signs and specimens
• Enter and verify study data in electronic data capture systems
• Maintain regulatory binders and ensure documentation is audit-ready
• Prepare and submit IRB applications, amendments, and continuing reviews
• Report adverse events and protocol deviations to investigators and sponsors
• Coordinate with sponsors, monitors, and laboratory staff during site visits
• Track study supplies, investigational product, and visit schedules

Requirements

• Bachelor's degree in life sciences, nursing, public health, or a related field
• 2 or more years of clinical research coordination experience
• Working knowledge of Good Clinical Practice (GCP) and FDA regulations
• Experience with electronic data capture and clinical trial management systems
• Strong organizational and documentation skills
• Clear written and verbal communication with participants and study teams
• CITI or equivalent human subjects research certification preferred
• Phlebotomy experience a plus

Benefits

• Medical, dental, and vision insurance
• 401(k) with employer match
• Paid time off and paid holidays
• Tuition and professional development assistance
• Pre-tax commuter benefits for MBTA
• Life and disability insurance
• Opportunities for advancement into senior research roles

Job Type: Full-Time | Work Type: On-Site | Industry: Healthcare | Experience: Associate