The Johns Hopkins University
Clinical Research Coordinator (Psychiatry & Behavioral Sciences)
The Johns Hopkins University, Baltimore, Maryland, United States, 21276
Clinical Research Coordinator (Psychiatry & Behavioral Sciences)
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Clinical Research Coordinator (Psychiatry & Behavioral Sciences)
role at
The Johns Hopkins University .
The Behavioral Pharmacology Research Unit is seeking a Clinical Research Coordinator who reports to the Sr. Clinical Research Manager.
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 recruitment techniques as appropriate (print and web‑based advertisements, contact referring physicians, community event participation, 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 or 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.
Technical Skills And 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
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.
Location: Johns Hopkins Bayview. Employment: Full Time (Monday through Friday, 40 hours). FLSA Status: Non‑Exempt.
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Clinical Research Coordinator (Psychiatry & Behavioral Sciences)
role at
The Johns Hopkins University .
The Behavioral Pharmacology Research Unit is seeking a Clinical Research Coordinator who reports to the Sr. Clinical Research Manager.
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 recruitment techniques as appropriate (print and web‑based advertisements, contact referring physicians, community event participation, 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 or 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.
Technical Skills And 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
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.
Location: Johns Hopkins Bayview. Employment: Full Time (Monday through Friday, 40 hours). FLSA Status: Non‑Exempt.
#J-18808-Ljbffr