Hybrid Clinical Research Coordinator — Trials & Compliance

Johns Hopkins University; Baltimore (MD); Hybrid; USD 24,000 - 42,000; Part time

Job summary

Johns Hopkins University is seeking a Clinical Research Coordinator to administratively coordinate protocol implementation for a single study and ensure efficient logistical execution. The role includes coordinating study activities, assisting staff, and supporting regulatory matters.

The position involves participant recruitment, data entry and management, and collaboration with investigators and nurses. A Bachelor's degree is required, and prior human subjects research experience is preferred.

Qualifications

• Bachelor's degree in a related field; substitutions allowed per policy.

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 staff in executing protocol-related activities.
• Explain the study background and rationale to participants.
• Assist with IRB submissions and regulatory communications.

Skills

Attention to Detail

Regulatory Compliance

Oral and Written Communications

Organizational Skills

Project Coordination

Interpersonal Skills

Education

Bachelor's Degree in related field

Tools

Clinical Trial Management System

Data Entry

Data Collection and Reporting

Data Management and Analysis

Job description

Johns Hopkins University is seeking a Clinical Research Coordinator to administratively coordinate protocol implementation for a single study and ensure efficient logistical execution. The role includes coordinating study activities, assisting staff, and supporting regulatory matters.

The position involves participant recruitment, data entry and management, and collaboration with investigators and nurses. A Bachelor's degree is required, and prior human subjects research experience is preferred.