Location: Washington, DC
Cap-Exempt H-1B Position — No lottery required
Affiliated Office Address **Washington, DC, United States** Requisition ID **121340** Date Created **May 21, 2026** Job Family **Research** Job Subfamily **General Research** Job Function **Research** Exempt Status **Non-Exempt** Shift Type **Full Time** Schedule **M-F, 8:30am-5:00pm** Worksite **01-DC:District of Columbia** Work Modality **On-site: 90-100% of hours worked on-site** Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We are seeking a ***Clinical Research Coordinator*** who will administratively coordinate 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. The Clinical Research Coordinator will monitor the clinical course and collection of research data on patients participating in clinical trials at the Johns Hopkins University-Sibley Hospital location, Department of Radiation Oncology. The Clinical Research Coordinator will manage patient clinical research data which will be used to generate specific study findings. **Specific Duties & 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