Clinical Research Coordinator I: Trial Operations

Dartmouth-Hitchcock Health; Lebanon (NH); On-site; USD 48,000 - 62,000; Full time

Job summary

Dartmouth-Hitchcock Health in Lebanon, NH seeks a Clinical Research Coordinator I to support basic clinical trial administrative tasks under direct supervision. The role emphasizes subject management, data entry in CTMS, and regulatory document handling to ensure study operations run smoothly.

You will gain exposure to IRB processes, sponsor communications, and on-site/off-site record maintenance, with the required bachelor’s degree and certifications as baseline.

Qualifications

• Bachelor's degree or equivalent education/experience.
• BLS certification within 30 days of hire.
• Clinical research experience preferred.
• Familiarity with IRB processes and Good Clinical Practice (GCP).

Responsibilities

• May arrange/schedule required appointments.
• Learns and supports all aspects of study operations with substantial oversight from the investigator or designee.
• Supports subject management, such as visit preparation, data entry in CTMS, scans informed consents into EMR.
• Assists with compiling/regulatory documents and sponsor communications.
• Maintains essential regulatory documents and supports IRB submissions and site visits.

Skills

Attention to detail

Effective communication

Team collaboration

Time management

Education

Bachelor's degree or equivalent education/experience

BLS certification within 30 days of hire

Tools

CTMS

EMR systems

IRB submission systems

Job description

Dartmouth-Hitchcock Health in Lebanon, NH seeks a Clinical Research Coordinator I to support basic clinical trial administrative tasks under direct supervision. The role emphasizes subject management, data entry in CTMS, and regulatory document handling to ensure study operations run smoothly.

You will gain exposure to IRB processes, sponsor communications, and on-site/off-site record maintenance, with the required bachelor’s degree and certifications as baseline.