Clinical Research Coordinator – Urology
John Hopkins University
full-time
Posted on:
Location Type: Office
Location: Baltimore • Maryland • 🇺🇸 United States
Visit company websiteSalary
💰 $17 - $30 per hour
Job Level
Mid-LevelSenior
About the role
- 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.
- Perform biospecimen collection, including blood draws and other sample types, following IRB-approved protocols and ensuring proper labeling and documentation.
- Process, aliquot, and store biological samples according to study-specific and biorepository SOPs to maintain specimen integrity and compliance with quality standards.
Requirements
- 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.
- Related undergraduate or work experience in human subject's research.
- 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.
Benefits
- Johns Hopkins offers a total rewards package that supports our employees' health, life, career and retirement.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
data entrydata collectiondata managementdata analysisbiospecimen collectionblood drawssample processingprotocol adherencerecruitment strategy developmentliterature searches
Soft skills
attention to detailinterpersonal skillsoral communicationwritten communicationorganizational skillsproject coordination