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Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We are seeking a **Clinical Research Coordinator** who will administratively coordinate 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.

The School of Medicine Division of Pediatric Endocrinology is seeking a Clinical Research Coordinator who will assist Dr. Hitt’s research is in the development and progression of prediabetes and type 2 diabetes in children, with a current focus on the relationship between sleep and metabolic dysfunction. The position will also assist Dr. Hitt with the development of future research studies in the area of pediatric insulin resistance, type 2 diabetes, and cardiometabolic risk. This position supports the research programs and/or clinical trials of pediatric endocrinologist, Dr. Talia Hitt.

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 clinical team, 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/participate in coordinating study meetings. which may include assisting in developing an agenda and coordinating information and/or participation of individuals from other institutions and/or universities.

+ 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.

+ Develop moderately complex tracking database/spreadsheet based on study requirements utilizing REDcap, Excel, or similar software applications.

+ Abstract data from patient medical records that may require some interpretation. Monitors data quality and accuracy as required by research protocol.

+ Conduct study visits which may include completion of case report forms, obtaining vital signs, and processing samples (blood, saliva, urine, and/or stool).

+ Utilizing working knowledge of study(s) will participate in meetings to provide operational updates, report on any operational issues, and may make recommendations for resolutions to new/outstanding operational issues.

+ Other duties as assigned.

_*May be required to work on multiple studies at the same time_

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 subject's research.

+ Prior clinical research experience, experience with REDCap, Excel, and coding.

Technical Qualifications & Specialized Certifications

_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 (SOM Pediatric Endocrinology)

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

Starting Salary Range: $17.20 - $30.30 HRLY ($26,800 targeted; Commensurate w/exp.)

Employee group: Casual / On Call

Schedule: M-F; days/hours may vary

FLSA Status: Non-Exempt

Department name: SOM Ped Endocrine

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.