Clinical Research Coordinator: Emergency Medicine HIV/STI Trials

The Johns Hopkins University; Baltimore (MD); On-site; USD 25,000 - 43,000; Full time

Job summary

The Johns Hopkins University in Maryland is seeking a Clinical Research Coordinator to support single- and multicenter infectious disease studies focusing on HIV, viral hepatitis, and STIs. You will recruit, screen, enroll participants, and assist with data management and regulatory submissions.

Responsibilities include coordinating protocol implementation, participating in study meetings, and liaising with IRB and study staff. On-call hours and flexible scheduling are required.

Qualifications

• Bachelor's Degree in a related field is required.
• Education may be substituted per equivalency rules.
• Experience in clinical research or public health programs is preferred.

Responsibilities

• Coordinate activities of a clinical research study to ensure adherence to protocol.
• Assist with start-up meetings and protocol-related activities.
• Explain study background and rationale to participants; assist in recruitment strategies.
• Conduct consenting process or obtain consent for appropriate participants.
• Enter and organize data; assist in coordinating study meetings and IRB submissions.
• Liaise with IRB on administrative matters and communicate with the PI.
• Oversee operating knowledge of assigned protocol and clinical systems.
• On-call and non-standard hours as required.

Skills

Attention to Detail

Clinical Trial Management

Data Entry

Data Collection

Data Management

Interpersonal Skills

Oral & Written Comm

Organizational Skills

Project Coordination

Regulatory Compliance

Education

Bachelor's Degree in related field

Job description

The Johns Hopkins University in Maryland is seeking a Clinical Research Coordinator to support single- and multicenter infectious disease studies focusing on HIV, viral hepatitis, and STIs. You will recruit, screen, enroll participants, and assist with data management and regulatory submissions.

Responsibilities include coordinating protocol implementation, participating in study meetings, and liaising with IRB and study staff. On-call hours and flexible scheduling are required.