We are seeking a Clinical Research Coordinator in the department of Otolaryngology. Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases …
Skills: Clinical research coordination, Protocol implementation, Regulatory compliance, Data collection, Data management
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Northrop Grumman Mission Systems, Inc.
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Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our coll…
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$17/hr–$31/hr
Full-time
bachelor degree
Posted 16d ago
~38 hrs/week
Responsibilities
The Clinical Research Coordinator manages the logistical implementation of clinical protocols and ensures adherence to study findings. They also provide administrative support for regulatory issues, participant recruitment, and data collection systems.
Requirements
Candidates must possess a Bachelor's degree in a related field. Previous experience in human subjects research is preferred.
Full job description
We are seeking a Clinical Research Coordinator in the department of Otolaryngology. 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 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 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.
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 Prefered.
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 Communications - 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 (Otolaryngology) Role/Level/Range: ACRO37.5/03/CD Starting Salary Range: $17.65 - $31.05 HRLY ($24.35/hour argeted; Commensurate w/exp.) Employee group: Full Time Schedule: M-F, 8am-5:30 FLSA Status: Non-Exempt Location: School of Medicine Campus Department name: SOM Oto Otolaryngology Research Personnel area: School of Medicine
The Johns Hopkins University was the first university in the Western Hemisphere based on the European research institution, with a mission both to teach and to advance human knowledge through discovery. Its establishment revolutionized U.S. higher education. Today, Johns Hopkins remains a world leader in education, research and patient care. It ranks first among U.S. universities in winning federal research and development funds.
Offices: 3400 N Charles St, Baltimore, Maryland 21218, US
How many Science & Research jobs are open in Baltimore, MD right now?
There are currently 886 open science & research positions in Baltimore, MD listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Baltimore, MD?
Companies currently hiring include John Hopkins University, University System of Maryland, Northrop Grumman, Northrop Grumman Mission Systems, Inc., University of Maryland Medical System, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Baltimore, MD?
Yes — 228 of the 886 open science & research positions offer remote or hybrid work (54 remote, 174 hybrid).
How do I apply for Science & Research jobs in Baltimore, MD?
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