Clinical Research Coordinator - Trials & Participants

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 clinical trials and studies at the School of Medicine. This role focuses on coordinating protocol implementation, logistics, and study-related regulatory tasks to ensure compliant, efficient execution.

Responsibilities include participant consent, recruitment support, data entry, and collaboration with investigators and study personnel to advance research aims.

Qualifications

• Bachelor's Degree in a related field required.
• Experience in clinical research preferred or required per job listing.
• Familiarity with IRB processes and study regulatory aspects.

Responsibilities

• Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
• Assist with IRB submissions and regulatory communications.
• Explain study background to participants and coordinate recruitment and consenting processes.
• Enter and organize data in study data collection systems and provide operational updates.

Skills

Clinical coordination

IRB submissions

Patient consent

Study logistics

Data entry

Education

Bachelor's Degree in related field

Tools

Electronic data capture (EDC) systems

Job description

The Johns Hopkins University is seeking a Clinical Research Coordinator to support clinical trials and studies at the School of Medicine. This role focuses on coordinating protocol implementation, logistics, and study-related regulatory tasks to ensure compliant, efficient execution.

Responsibilities include participant consent, recruitment support, data entry, and collaboration with investigators and study personnel to advance research aims.