Clinical Trials Coordinator — Behavioral Pharmacology

The Johns Hopkins University; Baltimore (MD); On-site; USD 23,419 - 41,328; Full time

Job summary

The Johns Hopkins University is seeking a Clinical Research Coordinator to support the Behavioral Pharmacology Research Unit at Johns Hopkins Bayview. You will coordinate protocol implementation, assist nurses and investigators, and ensure efficient study operations in a patient-centered environment.

Responsibilities include coordinating activities, obtaining consent, data entry, IRB submissions, and budget oversight. A Bachelor's degree is required; related research experience is preferred.

Qualifications

• Minimum: Bachelor's Degree in a related field.
• Education may substitute for experience per JHU policy.

Responsibilities

• Coordinate all activities of a clinical research study to ensure adherence to protocol.
• Assist research nurses and investigators in executing protocol-related activities.
• Explain study background and rationale to participants and recruit as needed.
• Obtain informed consent and schedule participant activities.
• Enter and organize data; assist in IRB submissions and liaison with IRB as needed.
• Maintain study documentation and budget oversight.
• Provide backup coverage for staff absences and scheduling conflicts.

Skills

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

Education

Bachelor's Degree in a related field

Tools

Clinical Trial Management System

Regulatory Compliance Tools

Job description

The Johns Hopkins University is seeking a Clinical Research Coordinator to support the Behavioral Pharmacology Research Unit at Johns Hopkins Bayview. You will coordinate protocol implementation, assist nurses and investigators, and ensure efficient study operations in a patient-centered environment.

Responsibilities include coordinating activities, obtaining consent, data entry, IRB submissions, and budget oversight. A Bachelor's degree is required; related research experience is preferred.