Clinical Research Coordinator — Hematology Trials

The Johns Hopkins University; Baltimore (MD); On-site; USD 24,000 - 43,000; Full time

Job summary

The Johns Hopkins University is seeking a Clinical Research Coordinator to administratively coordinate clinical protocol implementation for a study in the Hematologic Malignancies division. You will monitor patient data, assist with regulatory submissions, and ensure accurate data collection for cancer research.

Under supervision, you will support recruitment, consent, and scheduling of study activities, while liaising with IRB and research staff to maintain protocol integrity and data quality.

Qualifications

• Bachelor's Degree in a related field.
• Additional education may substitute for required experience or education per JHU policy.

Responsibilities

• Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
• Participate in start-up meetings and maintain knowledge of protocols and reporting requirements.
• Transmit protocol information and maintain protocol library data in the Clinical Research Management System.
• Assist nurses, coordinators, PIs and staff in executing protocol-related activities and consent participants.
• Verify patient eligibility, schedule activities, and liaison with participants and IRB on administrative matters.

Education

Bachelor's Degree in a related field

Job description

The Johns Hopkins University is seeking a Clinical Research Coordinator to administratively coordinate clinical protocol implementation for a study in the Hematologic Malignancies division. You will monitor patient data, assist with regulatory submissions, and ensure accurate data collection for cancer research.

Under supervision, you will support recruitment, consent, and scheduling of study activities, while liaising with IRB and research staff to maintain protocol integrity and data quality.