Cancer Research Coordinator I — Clinical Trials

Dartmouth-Hitchcock Health; Lebanon (NH); Vor Ort; USD 52.000 - 75.000; Vollzeit

Zusammenfassung

Dartmouth-Hitchcock Health is seeking a Clinical Research Coordinator I to support basic administrative clinical trial tasks under direct supervision of the Principal Investigator. The role involves subject management, data entry in CTMS, and regulatory activities.

You will assist with IRB submissions, maintain study documents, coordinate site visits, and ensure adherence to ICH-GCP guidelines and DHMC procedures.

Qualifikationen

• Bachelor's degree or equivalent required.
• Previous research experience preferred.
• BLS certification within 30 days of hire.
• IRB/GCP certificates within 30 days of hire.

Aufgaben

• Support study operations and subject management with substantial oversight.
• Perform data entry in CTMS and complete paper/eCRFs.
• Assist with regulatory submissions and sponsor communications.
• Coordinate site visits and communicate with investigators and stakeholders.

Kenntnisse

Communication skills

Attention to detail

Ausbildung

Bachelor's degree or equivalent

Tools

CTMS

EMR

EDC

Jobbeschreibung

Dartmouth-Hitchcock Health is seeking a Clinical Research Coordinator I to support basic administrative clinical trial tasks under direct supervision of the Principal Investigator. The role involves subject management, data entry in CTMS, and regulatory activities.

You will assist with IRB submissions, maintain study documents, coordinate site visits, and ensure adherence to ICH-GCP guidelines and DHMC procedures.