Clinical Research Coordinator — Hybrid Study Operations & Recruitment

Johns Hopkins University; Baltimore (MD); Hybrid; USD 36,000 - 54,000; Full time

Job summary

Johns Hopkins University in Baltimore seeks a Clinical Research Coordinator to administratively coordinate protocol implementation and provide regulatory support. The role focuses on efficient study logistics, enrollment, consent, and coordination with investigators and study staff.

The coordinator will handle data entry, IRB submissions, and budget oversight, while supporting recruitment activities and ensuring compliance with research regulations.

Qualifications

• Bachelor's Degree in a related field is required.
• Additional education may substitute for required experience.

Responsibilities

• Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
• Participate in clinical study start-up meetings.
• Assist researchers and staff in executing protocol-related activities.
• Explain the study background and rationale to participants.
• Coordinate recruitment strategies and conduct participant recruitment activities.
• Independently obtain informed consent where appropriate.
• Schedule participants for tests and provide instructions for upcoming activities.
• Serve as liaison to study participants and assist with data collection and meetings.
• Prepare IRB submissions and liaise with the IRB on administrative matters.
• Oversee study budget expenditures and maintain equipment and systems knowledge.

Education

Bachelor's Degree

Job description

Johns Hopkins University in Baltimore seeks a Clinical Research Coordinator to administratively coordinate protocol implementation and provide regulatory support. The role focuses on efficient study logistics, enrollment, consent, and coordination with investigators and study staff.

The coordinator will handle data entry, IRB submissions, and budget oversight, while supporting recruitment activities and ensuring compliance with research regulations.