Hybrid Oncology Clinical Research Coordinator

John Hopkin’s University; Maryland; Hybrid; USD 24,000 - 43,000; Full time

Job summary

Johns Hopkins University in Maryland seeks a Clinical Research Coordinator to coordinate protocol implementation and study activities, providing regulatory and logistical support. You will assist investigators, manage data, coordinate meetings, support participant recruitment, and oversee IRB submissions in a hybrid work setting on the School of Medicine campus.

Strong organizational skills and the ability to collaborate across clinical teams are essential for success.

Qualifications

• Bachelor's Degree in a related field.

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.
• Implement a variety of techniques for recruitment as appropriate, e.g., print and web-based advertisements, contact referring physicians, participate in community events, etc.
• 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.

Education

Bachelor's Degree in a related field

Job description

Johns Hopkins University in Maryland seeks a Clinical Research Coordinator to coordinate protocol implementation and study activities, providing regulatory and logistical support. You will assist investigators, manage data, coordinate meetings, support participant recruitment, and oversee IRB submissions in a hybrid work setting on the School of Medicine campus.

Strong organizational skills and the ability to collaborate across clinical teams are essential for success.