Research Project Coordinator (Pediatrics)
About The Position
The Pediatrics Department’s Adolescent Medicine division is seeking a Research Project Coordinator to administratively coordinate research protocol implementation, typically for a single study. The coordinator ensures efficient logistical implementation of study activities and provides administrative support for related matters. The role includes coordinating study activities, supporting research operations, and carrying out additional study-specific duties, including patient recruitment and enrollment, data analysis and entry, and IRB submissions. The position is scheduled Monday through Friday, 8:30 a.m. to 5 p.m., at the School of Medicine Campus.
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 or equivalent, as permitted by the JHU equivalency formula.
- Awareness-level administrative skills.
- Awareness-level data entry skills.
- Awareness-level interpersonal skills.
- Awareness-level literature review skills.
- Awareness-level oral and written communication skills.
- Awareness-level organizational skills.
- Awareness-level project coordination skills.
- Awareness-level research and analytical skills.
Nice To Haves
- Understanding of ME/CFS.
- Proficiency with EPIC, RedCap, and statistical software.
- Lived experience with ME/CFS.
Responsibilities
- Coordinate research study activities to ensure the validity of findings.
- Work with the Principal Investigator or senior research staff to develop operational plans that meet research goals.
- Develop tools and procedures for data collection and study processes.
- Collect and organize data according to study requirements, including participant interviews, questionnaire administration, background research, and laboratory processing.
- Ensure adherence to research protocols and procedures.
- Assist with setting up data collection systems and enter and organize data.
- Oversee research study record management.
- Oversee budget expenditures for study operations.
- Assist in coordinating study meetings.
- Participate in study meetings, report on protocol implementation status, and recommend solutions to operational issues.
- Conduct literature searches to provide background information.
- Recruit and enroll patients in the IRB-approved Cohort II study, the Ivabradine Study, the Neurogenic Thoracic Outlet Syndrome Study, and the pending High-Dose Oral Cromolyn study application.
- Analyze data for the Cohort II study.
- Complete data entry.
- Prepare IRB submissions.
- Perform other duties as assigned.
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What This Job Offers
Job Type
Full-time
