Clinical Research Trial Coordinator — Flexible Schedule

Beth Israel Lahey Health; Burlington (MA); On-site; USD 26,000 - 43,000; Full time

Job summary

Beth Israel Lahey Health in Massachusetts is seeking a Clinical Research Coordinator to screen and enroll patients in clinical trials, monitor adherence to protocols, and complete required documentation. The role supports data collection and coordination across study sites while ensuring patient safety and regulatory compliance.

Responsibilities include identifying eligible subjects, obtaining informed consent, scheduling visits, and assisting with insurance approvals.

Qualifications

• Bachelor's degree required in a related field.
• 1-2 years of related work experience required.
• Medical terminology knowledge is required.
• Working knowledge of computer systems and MS Office applications.

Responsibilities

• Screen and enroll patients onto clinical trials per protocol.
• Monitor protocol implementation and complete required forms.
• Extract data from records and enter into the data system.
• Assist with insurance approvals and scheduling tests as needed.
• Communicate with IRB and study staff as required.

Skills

Medical terminology

Attention to detail

Problem solving

Education

Bachelor's degree

Tools

Microsoft Office

Web-based applications

Job description

Beth Israel Lahey Health in Massachusetts is seeking a Clinical Research Coordinator to screen and enroll patients in clinical trials, monitor adherence to protocols, and complete required documentation. The role supports data collection and coordination across study sites while ensuring patient safety and regulatory compliance.

Responsibilities include identifying eligible subjects, obtaining informed consent, scheduling visits, and assisting with insurance approvals.