Johns Hopkins University·Washington, District of Columbia
The coordinator manages the administrative and logistical implementation of clinical research protocols in the Urology department. Key duties include participant recruitment, consenting, data collection, and the processing and tracking of biospecimens.
We are seeking a Clinical Research Coordinator in the department of Urology at Sibley Memorial Hospital. Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. The Clinical Research Coordinator administratively coordinates clinical protocol implementation, typically for a single study. Will ensure efficient logistical implementation of the study activities and provide administrative support for research-related regulatory issues.
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.
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.
Related undergraduate or work experience in human subjects' research is preferred.
Technical Skills & Expected Level of Proficiency Attention to Detail - Awareness Clinical Trial Management System - Awareness Data Entry - Awareness Data Collection and Reporting - Awareness Data Management and Analysis - Awareness Interpersonal Skills - Awareness Oral and Written Communications - Awareness Organizational Skills - Awareness Project Coordination - Awareness Regulatory Compliance - Awareness
The core technical skills listed are most essential; additional technical skills may be required based on specific division or department needs. Classified Title: Clinical Research Coordinator Role/Level/Range: ACRO40/E/03/CD Starting
$17.20 - $30.30 HRLY ($23.75/hour targeted; Commensurate w/exp.) Employee group: Full Time Schedule: M-F; 8am-4:30pm FLSA Status: Non-Exempt Location: District of Columbia Department name: Urology Personnel area: School of Medicine
A Bachelor's degree in a related field is required, with a preference for candidates having undergraduate or work experience in human subjects' research. Proficiency in regulatory compliance and clinical data management is expected.
Market context
Clinical research coordinator roles in urology in the District of Columbia are typically driven by active hospital, academic, and specialty-clinic research programs, so openings can be competitive when they require both regulatory compliance and clinical data management skills. Candidates with a bachelor’s degree and prior human subjects’ research experience often stand out. Review the AI-summarized requirements and benefits on this page against the original posting, then tailor your application to show direct experience with consent, documentation, and study coordination.
