Urology Clinical Research Coordinator: Trials

The Johns Hopkins University; Baltimore (MD); On-site; USD 50,574,000 - 88,971,000; Full time

Job summary

The Johns Hopkins University in Baltimore seeks a Clinical Research Coordinator (Urology) to manage protocol implementation, assist with regulatory tasks, and coordinate participant recruitment and scheduling. The role involves liaising with investigators, nurses, and participants to ensure compliant, efficient study operations.

Responsibilities include consent, data entry, biospecimen coordination, and IRB submissions, with a focus on quality and regulatory adherence in a fast-paced research

Qualifications

• Bachelor's Degree in a related field.
• Education substitutions may apply per JHU equivalency formula.

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 researchers and staff in executing protocol-related activities.
• Explain study background and rationale to participants.
• Recruit participants using various strategies (ads, referrals, community events).
• Obtain informed consent and schedule participant activities.
• Serve as liaison to participants and coordinate study communications.
• Set up data collection systems and enter data.
• Assist with study meetings and protocol implementation updates.
• Prepare IRB submissions and liaise on administrative matters.
• Maintain literature background and knowledge of study protocol and equipment.

Skills

Attention to Detail

Clinical Trial Management System

Data Entry

Data Collection and Reporting

Data Management and Analysis

Interpersonal Skills

Oral and Written Communications

Organizational Skills

Project Coordination

Regulatory Compliance

Education

Bachelor's Degree in a related field

Job description

The Johns Hopkins University in Baltimore seeks a Clinical Research Coordinator (Urology) to manage protocol implementation, assist with regulatory tasks, and coordinate participant recruitment and scheduling. The role involves liaising with investigators, nurses, and participants to ensure compliant, efficient study operations.

Responsibilities include consent, data entry, biospecimen coordination, and IRB submissions, with a focus on quality and regulatory adherence in a fast-paced research