Clinical Research Coordinator (Research Administration)

Johns Hopkins University; Baltimore (MD); On-site; USD 23,694 - 41,741; Part time

Job summary

A prominent research institution seeks a Clinical Research Coordinator to manage various aspects of clinical studies. Duties include coordinating study activities, assisting in recruitment, and ensuring adherence to protocols. A Bachelor's degree is required, and prior experience in human subject research is preferred. This part-time role offers a flexible schedule and a salary range of $17.20 - $30.30 per hour, based on experience.

Qualifications

• Bachelor's degree in a related field.
• Experience in human subject research is preferred.

Responsibilities

• Coordinate all activities of a clinical research study.
• Assist with recruiting participants.
• Conduct literature searches for background information.

Skills

Attention to Detail

Interpersonal Skills

Oral and Written Communications

Organizational Skills

Project Coordination

Education

Bachelor's Degree in a related field

Job description

Overview

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.

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 Johns Hopkins University equivalency formula.

Preferred Qualifications

• Related undergraduate or work experience in human subject research.

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 (Research Administration)
Role/Level/Range: ACRO37.5/03/CD
Starting Salary Range: $17.20 - $30.30 HRLY ($24,398.40 targeted; Commensurate w/exp.)
Employee group: Part-time
Schedule: Monday - Friday (20 hours per week)
FLSA Status: Non-Exempt
Location: School of Nursing (Baltimore, MD)
Department name: 60009277-Research Administration
Personnel area: School of Nursing