Research Program Coordinator

Johns Hopkins University

Posted 2 months ago

Full Time

Baltimore, Maryland

In Person

Smart Summary

Responsibilities

The Research Program Coordinator will manage the administrative and logistical implementation of clinical research protocols. Responsibilities include participant recruitment, data collection, regulatory submission assistance, and ensuring adherence to study protocols.

Qualifications

You have a Bachelor's degree in a related field and possess an awareness of skills such as clinical trial management, data entry, and regulatory compliance. You will coordinate clinical research activities, ensure adherence to protocols, manage study logistics, and provide administrative support for regulatory matters.

Must Have Skills for ATS

Clinical Trial Management System

Data Entry

Data Collection and Reporting

Data Management and Analysis

Project Coordination

Regulatory Compliance

Job Description

Researchers at Johns Hopkins University is seeking a Research Program Coordinator to 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 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.

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


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.

Classified Title: Research Project Coordinator 
Job Posting Title (Working Title): Research Program Coordinator (Psychiarty and Behavioral Sciences)   
Role/Level/Range: ACRO40/E/03/CD  
Starting Salary Range: $17.20 - $30.30 HRLY ($41,820 targeted; Commensurate w/exp.) 
Employee group: Full Time 
Schedule: Monday-Friday/8:30A-5:00P 
FLSA Status: Non-Exempt 
Location: School of Medicine Campus  
Department name: SOM Psy Affect Disorders and Psych Genet   
Personnel area: School of Medicine 

Johns Hopkins University

The Johns Hopkins University was the first university in the Western Hemisphere based on the European research institution, with a mission both to teach and to advance human knowledge through discovery. Its establishment revolutionized U.S. higher education. Today, Johns Hopkins remains a world leader in education, research and patient care. It ranks first among U.S. universities in winning federal research and development funds.
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