Ophthalmology Clinical Research Coordinator II

The Johns Hopkins University; Baltimore (MD); On-site; USD 28,000 - 50,000; Full time

Job summary

The Johns Hopkins University in Baltimore, MD, seeks a Clinical Research Coordinator II to administratively coordinate the implementation of a complex clinical protocol or multiple studies. You will support study teams, recruit participants, obtain consent, and ensure regulatory compliance.

Responsibilities include coordinating start-up activities, data collection, IRB submissions, budget oversight, and collaboration with nurses, investigators, and external partners.

Qualifications

• Bachelor's Degree in related field.
• One year of related experience.
• Additional education may substitute for required experience and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent.

Responsibilities

• Coordinate activities of a complex clinical study to ensure adherence to protocol.
• Assist with start-up meetings and the consenting process for participants.
• Explain the study background and rationale to potential and current participants.
• Develop recruitment strategies and conduct participant recruitment for one or more studies.
• Prepare IRB submissions and maintain regulatory documentation.
• Enter and organize data; assist with data collection systems and study meetings.
• Oversee study budgets and ensure adequate supplies are ordered and maintained.
• Train and oversee other non-exempt study staff as needed.

Skills

Budget Management

Clinical Research Knowledge

Clinical Trial Management System

Data Collection and Reporting

Good Clinical Practices

Interpersonal Skills

Project Coordination

Regulatory Compliance

Information Gathering

Education

Bachelor's Degree in related field

Job description

The Johns Hopkins University in Baltimore, MD, seeks a Clinical Research Coordinator II to administratively coordinate the implementation of a complex clinical protocol or multiple studies. You will support study teams, recruit participants, obtain consent, and ensure regulatory compliance.

Responsibilities include coordinating start-up activities, data collection, IRB submissions, budget oversight, and collaboration with nurses, investigators, and external partners.