
Clinical Research Coordinator (SOM Pediatric Young Adult & Adolescent Medicine) - #Staff
Baltimore, MDPer Diem$17.65–31.05/hrSeen 4 days agoSeen in employer's feed 4 days ago
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At a glance
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Job overview
Johns Hopkins University seeks a Clinical Research Coordinator for the School of Medicine’s Pediatric and Young Adult Medicine. The coordinator administratively supports clinical protocol implementation, study logistics, and research-related regulatory matters, typically for a single study. The role also supports participant recruitment and follow-up, data management, and text-messaging systems.
Skills & qualifications
Skills
Qualifications
Full job description
Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. School of Medicine, Pediatric and Young Adult Medicine is seeking a Clinical Research Coordinator to administratively coordinates 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.
Specific Duties & Responsibilities
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Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
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Participate in clinical study start-up meetings.
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Assist research nurses, study coordinators, principal investigators, and other study personnel in executing protocol-related activities.
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Explain the study background and rationale for the research to potential and current participants
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Contribute to the development of recruitment strategies for participants for assigned study.
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Implement a variety of techniques for recruitment as appropriate, e.g., print and web-based advertisements, contact referring physicians, participate in community events, etc.
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Independently conduct the consenting process or ensure consent is obtained on appropriate participants.
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Schedule participants for required activities and provide any special instructions prior to upcoming tests/exams.
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Serve as liaison to study participants.
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Assist with setup of the data collection system and enter and organize data.
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Assist in coordinating study meetings.
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Participate in study meetings and provide updates on protocol implementation status and make recommendations on operational issues.
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Assist with the preparation of submissions to the Institutional Review Board (IRB)
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Liaison with IRB on administrative matters and facilitate communications with the PI.
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Conduct literature searches to provide background information.
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Obtain and maintain excellent operating knowledge of assigned clinical protocol, clinical equipment, and clinical computer systems.
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Oversee budget expenditures for study operations.
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Other duties as assigned.
In addition to the duties described above
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Help build and manage text messaging system
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Track participants over time, including monitoring of responses in text messaging platform/study email account, and interim and end-of-study in-person and phone follow-up contact.
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Assist with data management for research, using Excel, RedCap, or similar system, and set up / monitor any additional database(s).
Minimum Qualifications
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Bachelor's Degree in a related field.
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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
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Prior experience working with Engage Spark – text-messaging platform to use with intervention.
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Experience with behavioral clinical trial procedures
Technical Skills & Expected Level of Proficiency
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Attention to Detail - Awareness
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Clinical Trial Management System - Awareness
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Data Entry - Awareness
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Data Collection and Reporting - Awareness
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Data Management and Analysis - Awareness
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Interpersonal Skills - Awareness
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Oral and Written Communications - Awareness
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Organizational Skills - Awareness
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Project Coordination - Awareness
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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
Role/Level/Range: ACRO37.5/03/CD
Starting Salary Range: $17.65 - $31.05 HRLY ($25.00 targeted; Commensurate w/exp.)
Employee group: Casual / On Call
Schedule: Days and hours will vary
FLSA Status: Non-Exempt
Location: School of Medicine Campus
Department name: SOM Ped Adolescent Medicine
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.
How this job compares
Set against the 633 open Clinical Research Coordinator jobs on Olive Jobs, counted October 27, 2026.
- Pay
- This posting$17.65–31.05/hr
- US median$24–36/hr183 hourly ranges
This range's midpoint, $24.35/hr, is 19% below the US median midpoint ($30/hr) — in the lowest quarter of Clinical Research Coordinator hourly ranges across the US.
- Openings
- Olive Jobs lists 32 open Clinical Research Coordinator jobs in Maryland and 633 across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most in Maryland
- Johns Hopkins University (this employer)22 open
- Trinity Health4 open
- Experience
- Clinical Research Coordinator postings that state a minimum ask for 2 years of experience at the median; the middle half ask for 1 to 3 years (417 postings).
- Education
- 204 of the 633 open Clinical Research Coordinator jobs (32%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on October 27, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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