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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 the efficient logistical implementation of the study activities and provide administrative support for research-related regulatory issues.

We are seeking a **_Clinical Research Coordinator_** who will assist the research team with the conduct of pharmaceutical-sponsored clinical trials, long-term NIH-funded or other investigator-initiated research protocols examining the treatment and progression of disease in adults with HIV, hepatitis, COVID and other infectious diseases. The research will take place on the East Baltimore and Bayview Campuses.

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 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.

_In addition to the duties described above_

+ Coordinate site initiation visits for studies where Johns Hopkins is a participating site in a multisite study, a single site for an investigator-initiated study, or is the coordinating center and a Hopkin PI is the lead or protocol chair.

Minimum 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.

Preferred Qualifications

+ Related undergraduate or work experience in human subjects research.

Classified Title: Clinical Research Coordinator

Role/Level/Range: ACRO37.5/03/CD

Starting Salary Range: $17.20 - $30.30 HRLY ($49,400 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: Monday-Friday 8:30-5pm

FLSA Status: Non-Exempt

Department name: SOM DOM Infectious Disease

Personnel area: School of Medicine

Equal Opportunity Employer

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.