Hybrid Clinical Research Coordinator | Study Operations

John Hopkin’s University; Baltimore (MD); Hybrid; USD 24,000 - 43,000; Full time

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

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.