The Johns Hopkins University
Clinical Research Coordinator (DOM Infectious Disease)
The Johns Hopkins University, Baltimore, Maryland, United States, 21276
Clinical Research Coordinator (DOM Infectious Disease)
Researchers at Johns Hopkins University conduct clinical trials and studies to discover new ways to prevent and treat diseases such as HIV, hepatitis, COVID, and other infectious conditions. The Clinical Research Coordinator administratively coordinates clinical protocol implementation for a single study, ensuring efficient logistical implementation and providing 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. 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 studies.
Implement a variety of recruitment techniques, e.g., print and web‑based advertisements, contact referring physicians, participate in community events.
Independently conduct the consenting process or ensure consent is obtained from 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, making recommendations on operational issues.
Assist with 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.
Additional Duties
Coordinate site initiation visits for studies where Johns Hopkins is a participating site in a multisite study, a single‑site investigator‑initiated study, or is the coordinating center, and a Hopkins 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, 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 with experience)
Employee Group: Full Time
Schedule: Monday‑Friday 8:30‑5pm
FLSA Status: Non‑Exempt
Location: School of Medicine Campus
Department: School of Medicine DOM Infectious Disease
Personnel Area: School of Medicine
#J-18808-Ljbffr
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. 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 studies.
Implement a variety of recruitment techniques, e.g., print and web‑based advertisements, contact referring physicians, participate in community events.
Independently conduct the consenting process or ensure consent is obtained from 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, making recommendations on operational issues.
Assist with 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.
Additional Duties
Coordinate site initiation visits for studies where Johns Hopkins is a participating site in a multisite study, a single‑site investigator‑initiated study, or is the coordinating center, and a Hopkins 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, 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 with experience)
Employee Group: Full Time
Schedule: Monday‑Friday 8:30‑5pm
FLSA Status: Non‑Exempt
Location: School of Medicine Campus
Department: School of Medicine DOM Infectious Disease
Personnel Area: School of Medicine
#J-18808-Ljbffr