Dermatology Clinical Research Coordinator I

Dartmouth-Hitchcock Health; Lebanon (NH); On-site; USD 50,000 - 70,000; Full time

Job summary

Dartmouth-Hitchcock Health in Lebanon, NH seeks a Clinical Research Coordinator I to support study operations under the direct supervision of the Principal Investigator. You will assist with subject management, data entry in CTMS, regulatory submissions, and document control for IRB and sponsor requirements.

The role emphasizes adherence to ICH-GCP, ethics, and data quality; prior research experience is preferred, and a Bachelor's degree is required.

Qualifications

• Bachelor's degree or the equivalent combination of education and experience required.
• Previous research experience preferred.
• BLS certification and regulatory certificates must be obtained within 30 days of hire.

Responsibilities

• May arrange/schedule required appointments.
• Learns and supports all aspects of study operations with substantial oversight from the investigator or designee.
• Primarily supports subject management, such as subject visit preparation and data entry in the CTMS.
• Assists with compiling and maintaining essential records and documents for IRB submissions and sponsor requirements.
• Provides support to supervisor and IRB regarding regulatory and sponsor-related issues.
• Maintains and tracks regulatory documents per ICH-GCP guidelines.
• Assists with local and commercial IRB submissions, site visits, and document tracking.

Education

Bachelor's degree or the equivalent combination of education and experience required.

BLS certification within 30 days of hire date.

Human Subject Protection, Responsible Conduct of Research and Good Clinical Practice certificates required within 30 days of hire.

Job description

Dartmouth-Hitchcock Health in Lebanon, NH seeks a Clinical Research Coordinator I to support study operations under the direct supervision of the Principal Investigator. You will assist with subject management, data entry in CTMS, regulatory submissions, and document control for IRB and sponsor requirements.

The role emphasizes adherence to ICH-GCP, ethics, and data quality; prior research experience is preferred, and a Bachelor's degree is required.