Research Program Coordinator (Center for Psychedelic & Consciousness Research) - #Staff

Johns Hopkins University; Baltimore (MD); Hybride; USD 37 000 - 65 000; Plein temps

Résumé du poste

Johns Hopkins University is seeking a Research Program Coordinator for the Center for Psychedelic & Consciousness Research. The role oversees day-to-day activities of research projects, including recruitment, screening, and data collection, under the PI and Sr.

Clinical Research Coordinator. Responsibilities include coordinating study activities, assisting with IRB submissions, participant consent, and budget oversight.

Qualifications

• Bachelor's degree in a related field.
• Additional education may substitute for required experience per policy.

Responsabilités

• Coordinate all activities of a clinical research study to ensure adherence to protocol.
• Assist with participant recruitment, enrollment, and consent.
• Assist study personnel in executing protocol-related activities.
• Explain study background and rationale to participants.
• Contribute to recruitment strategy and implement recruitment methods.
• Schedule participants and provide pre-test instructions.
• Serve as liaison to study participants and coordinate data collection.
• Prepare IRB submissions and liaise with IRB as needed.
• Oversee study budget expenditures and financial tracking.

Connaissances

Attention to Detail

Clinical Trial Management System

Data Entry

Data Collection and Reporting

Data Management and Analysis

Interpersonal Skills

Oral and Written Communications

Organizational Skills

Project Coordination

Regulatory Compliance

Formation

Bachelor's Degree in related field

Master's Degree in related field

Description du poste

The Center for Psychedelic and Consciousness Research is seeking a Research Program Coordinato r who will oversee day to day activities of research projects including recruitment, screening, and data collection under the direction of the Principal Investigator and supervision of the Sr. Clinical Research Coordinator. 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 the 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 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.

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.

• Master's Degree in a related field.

Technical Skills and 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): Research Program Coordinator (Center for Psychedelic & Consciousness Research)

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

Starting Salary Range: $17.65 - $31.05 HRLY ($45,000 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: M-F 9-5:30

FLSA Status: Non-Exempt

Location: Hybrid/Johns Hopkins Bayview

Department name: PSYCHIATRY CPCR

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.