Hybrid Clinical Research Coordinator — Drive Clinical Trials

John Hopkin’s University; Baltimore (MD); Hybrid; USD 24,000 - 43,000; Full time

Job summary

Johns Hopkins University in Baltimore, MD, is seeking a Clinical Research Coordinator to administratively coordinate protocol implementation for a study, ensuring efficient logistics and regulatory support.

You will work with researchers, nurses, and PI, manage recruitment, consent, data entry, IRB submissions, and study meetings, with a Monday–Friday schedule and hybrid/Bayview location.

Qualifications

• 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/graduation equivalent, to the extent permitted by the JHU equivalency formula.

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 research nurses, study coordinators, principal investigators, and other study personnel in executing protocol-related activities.
• Explain the study background and rationale for the research to potential and current participants.
• Contribute to the development of recruitment strategies for participants for assigned study.
• Independently conduct the consenting process or ensure consent is obtained on appropriate participants.
• Schedule participants for required activities and provide any special instructions prior to upcoming tests/exams.
• Serve as liaison to study participants.
• Assist with setup of the data collection system and enter and organize data.
• Assist in coordinating study meetings.
• Participate in study meetings and provide updates on protocol implementation status and make recommendations on operational issues.
• Assist with the preparation of submissions to the Institutional Review Board (IRB)
• Liaison with IRB on administrative matters and facilitate communications with the PI.
• Conduct literature searches to provide background information.
• Obtain and maintain excellent operating knowledge of assigned clinical protocol, clinical equipment, and clinical computer systems.
• Oversee budget expenditures for study operations.
• Other duties as assigned.

Skills

Attention to Detail

CTMS Awareness

Data Entry

Data Collection

Data Management

Interpersonal Skills

Oral & Written Comm

Organizational Skills

Project Coordination

Regulatory Compliance

Education

Bachelor's Degree in a related field

Tools

Clinical Trial Management System

Job description

Johns Hopkins University in Baltimore, MD, is seeking a Clinical Research Coordinator to administratively coordinate protocol implementation for a study, ensuring efficient logistics and regulatory support.

You will work with researchers, nurses, and PI, manage recruitment, consent, data entry, IRB submissions, and study meetings, with a Monday–Friday schedule and hybrid/Bayview location.