Clinical Research Coordinator (The Institute for Clinical and Translational Research)

John Hopkin’s University

Baltimore (MD)

Hybrid

USD 24,000 - 43,000

Full time

3 hours ago

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Job summary

Johns Hopkins University is seeking a Clinical Research Coordinator to administratively coordinate protocol implementation for typically a single study. The role ensures efficient logistical execution and provides administrative support for regulatory matters.

The responsibilities include coordinating study activities, assisting in IRB submissions, liaising with participants, and maintaining data systems. A Bachelor's degree is required; related experience is preferred.

Qualifications

Bachelor's Degree in a related field (minimum).
Experience in human subjects' research preferred or related work experience.

Responsibilities

Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
Assist in start-up meetings and coordinate study operations.
Support nurses, coordinators and investigators in executing protocol-related activities.
Explain study background and rationale to participants.
Develop and implement recruitment strategies for study participants.

Skills

Attention to detail

Data entry

Regulatory compliance

Project coordination

Interpersonal skills

Oral & written communication

Organizational skills

Clinical trial management system

Education

Bachelor's degree

Tools

CTMS

Job description

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 JHU equivalency formula.

Preferred Qualifications