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Clinical Research Coordinator (Psychiatry & Behavioral Sciences) - #Staff

Johns Hopkins University

Baltimore, MDFull-time$17.65–31.05/hrSeen 1w agoSeen in employer's feed 4 days ago

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At a glance

Compensation
$17.65–31.05/hr
Location
Baltimore, MD
Schedule
Full-time
Work Authorization
Not specified

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Job overview

The Behavioral Pharmacology Research Unit seeks a Clinical Research Coordinator to administratively coordinate clinical protocol implementation, typically for a single study. The coordinator supports logistical study activities and research-related regulatory matters, working with study personnel and participants. The role also supports recruitment, consent, data collection, IRB communications, study documentation, and preparation of reports and presentations.

Skills & qualifications

RequiredNice to have

Skills

Attention to DetailClinical Trial Management SystemData EntryData Collection and ReportingData Management and AnalysisInterpersonal SkillsOral and Written CommunicationOrganizational SkillsProject CoordinationRegulatory ComplianceHuman Subjects Research

Qualifications

Bachelor's Degree in Related FieldRelated Human Subjects Research Experience

Full job description

The Behavioral Pharmacology Research Unit is seeking a Clinical Research Coordinator who reports to the Sr. Clinical Research Manager.

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.

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 meeting.

  • 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 strategy 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

  • Ensure the availability of test area facilities, supplies, and required protocol personnel in preparation for participant visits.

  • Implement protocol changes and ensure that the study team is appropriately trained.

  • Ensure appropriate study documentation.

  • Prepare study materials for bi-annual quality assurance checks.

  • Assist with the preparation of study reports, publications, and presentations.

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.

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 Communication - 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

Job Posting Title (Working Title): Clinical Research Coordinator (Psychiatry & Behavioral Sciences)

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

Starting Salary Range: $17.65 - $31.05 HRLY ($41,500 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: Monday thru Friday 8:30am 5:00pm

FLSA Status: Non-Exempt

Location: Johns Hopkins Bayview

Department name: SOM Psy Bay Behavioral Pharm Rserch Unit

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.

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