Clinical Research Coordinator I: Start in Trials & Data

Dartmouth Health; Lebanon (NH); On-site; USD 26,000 - 41,000; Full time

Job summary

Dartmouth Health is seeking a Clinical Research Coordinator I to support study operations under the supervision of the Principal Investigator. This role emphasizes regulatory compliance, data entry in CTMS, and coordination of site activities.

Responsibilities include assisting with regulatory submissions, maintaining essential documents, coordinating site visits, and ensuring data quality in CTMS and CRFs.

Qualifications

• Bachelor's degree or equivalent combination of education and experience required.
• Previous research experience preferred.
• 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.

Responsibilities

• Arrange and schedule required appointments.
• Support all study operations with oversight from the investigator or designee.
• Assist with subject management and data entry in CTMS; scan informed consents into EMR.
• Assist with compiling and maintaining essential regulatory documents for IRB submissions and sponsor communications.
• Maintain on-site and off-site storage of study records and tracking of essential documents.
• Assist with local and commercial IRB submissions, modifications, renewals, and closeout procedures.
• Follow ICH GCP guidelines and ensure data integrity and security.
• Complete all required training and adhere to professional guidelines.

Education

Bachelor's degree or equivalent

Job description

Dartmouth Health is seeking a Clinical Research Coordinator I to support study operations under the supervision of the Principal Investigator. This role emphasizes regulatory compliance, data entry in CTMS, and coordination of site activities.

Responsibilities include assisting with regulatory submissions, maintaining essential documents, coordinating site visits, and ensuring data quality in CTMS and CRFs.