Clinical Research Coordinator (The Institute for Clinical and Translational Research)

Johns Hopkins University • Baltimore, MD

6h • $18 - $31 • Hybrid

About The Position

The Clinical Research Coordinator administratively coordinates clinical protocol implementation, typically for a single study. The role ensures efficient logistical implementation of study activities and provides administrative support for research-related regulatory issues. The coordinator works with research nurses, study coordinators, principal investigators, and other study personnel to carry out protocol activities and support the study’s recruitment, participant engagement, data collection, regulatory processes, meetings, and budget operations.

Requirements

• Bachelor's degree in a related field.
• Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma or equivalent, as permitted by the JHU equivalency formula.

Nice To Haves

• Related undergraduate or work experience in human subjects' research.

Responsibilities

• Coordinate clinical research study activities to ensure adherence to protocol and validity of findings.
• Participate in clinical study start-up meetings.
• Assist research nurses, study coordinators, principal investigators, and other study personnel with protocol-related activities.
• Explain study background and rationale to potential and current participants.
• Contribute to developing participant recruitment strategies and implement appropriate recruitment techniques, such as print and web advertisements, contacting referring physicians, and participating in community events.
• Conduct the consenting process independently or ensure consent is obtained from appropriate participants.
• Schedule participants for required activities and provide special instructions before tests or examinations.
• Serve as a liaison to study participants.
• Assist with setting up the data collection system and entering and organizing data.
• Assist in coordinating study meetings, participate in them, provide updates on protocol implementation, and recommend operational improvements.
• Assist with preparing submissions to the Institutional Review Board (IRB).
• Liaise with the IRB on administrative matters and facilitate communications with the principal investigator.
• Conduct literature searches to provide background information.
• Maintain excellent operating knowledge of the assigned clinical protocol, clinical equipment, and clinical computer systems.
• Oversee budget expenditures for study operations.
• Perform other duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level