Clinical Research Coordinator: Lead Protocol Execution

Johns Hopkins University; Baltimore (MD); On-site; USD 50,574,000 - 88,971,000; Full time

Job summary

Johns Hopkins University is seeking a Clinical Research Coordinator to administratively coordinate clinical protocol implementation, typically for a single study, and provide administrative support for regulatory issues.

Responsibilities include coordinating study activities, assisting with recruitment, consenting, data management, IRB submissions, and liaison with participants and study team. Located at the School of Medicine Campus, schedule is Mon-Fri, 8:30am-5:00pm.

Qualifications

• Bachelor's degree in a related field.
• Education alternatives may substitute for experience per JHU policy.

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 development of recruitment strategies for participants for assigned study.
• Implement recruitment techniques such as ads, physician referrals, and community events.
• Independently conduct the consenting process or ensure consent is obtained on appropriate participants.
• Schedule participants for required activities and provide special instructions before tests/exams.
• Serve as liaison to study participants.
• Assist with setup of data collection system and enter data.
• Assist in coordinating study meetings and provide protocol updates.
• Assist with submissions to the IRB and liaise on administrative matters with the PI.
• Conduct literature searches for background information.
• Maintain knowledge of assigned clinical protocol, equipment, and computer systems.
• Oversee budget expenditures for study operations.
• Other duties as assigned.

Education

Bachelor's Degree in a related field

Job description

Johns Hopkins University is seeking a Clinical Research Coordinator to administratively coordinate clinical protocol implementation, typically for a single study, and provide administrative support for regulatory issues.

Responsibilities include coordinating study activities, assisting with recruitment, consenting, data management, IRB submissions, and liaison with participants and study team. Located at the School of Medicine Campus, schedule is Mon-Fri, 8:30am-5:00pm.