Clinical Research Coordinator II — Cancer Center

Dartmouth Health; Lebanon (NH); On-site; USD 46,000 - 72,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Paid time off

Retirement plans

Job summary

Dartmouth Health seeks a Clinical Research Coordinator II to manage study operations, data entry, and regulatory tasks under the PI. The role supports participant management, consent processes and QC of study data, with collaboration across IRBs, sponsors and investigators.

The position requires a Bachelor's degree with 2+ years of research experience, willingness to travel, and certification eligibility (SOCRA/ACRP). Commitment to GCP and patient safety is essential.

Qualifications

• Bachelor's degree with 2+ years of relevant research experience or equivalent.
• Ability to travel as required.
• SOCRA/ACRP Certification or eligible for certification preferred.
• BLS certification within 30 days of hire.
• Certifications in Human Subject Protection, Responsible Conduct of Research and Good Clinical Practice within 30 days.

Responsibilities

• Coordinate and support study operations, subject management and regulatory tasks under PI oversight.
• Data entry in CTMS, and entry of data into eCRFs per protocol.
• Administer QoL questionnaires under supervision and collect source data from medical records.
• Prepare regulatory documents and maintain study documentation.
• Interact with IRBs, sponsors and regulatory committees as needed.
• Communicate with participants and provide education and support to families.
• Assist with manuscript/abstract development and recruitment procedures.

Skills

Travel ability

Certification preferred

Bachelor's degree with experience

Education

Bachelor's degree

Job description

Dartmouth Health seeks a Clinical Research Coordinator II to manage study operations, data entry, and regulatory tasks under the PI. The role supports participant management, consent processes and QC of study data, with collaboration across IRBs, sponsors and investigators.

The position requires a Bachelor's degree with 2+ years of research experience, willingness to travel, and certification eligibility (SOCRA/ACRP). Commitment to GCP and patient safety is essential.