Senior Clinical Research Coordinator - Multicenter Trials

The Johns Hopkins University; Baltimore (MD); On-site; USD 42,000 - 74,000; Full time

Job summary

The Johns Hopkins University in Baltimore is seeking a Sr. Clinical Research Coordinator to oversee day-to-day operations of complex clinical studies, coordinating protocol activities, data collection, budgets, and regulatory compliance.

You will lead recruitment efforts, develop SOPs, prepare materials for IRB submission, collaborate with investigators across sites, and ensure data integrity and study milestones are met at Johns Hopkins Bayview.

Qualifications

• Bachelor's Degree in a related field.
• Three years of related experience.
• Additional education may substitute for required experience as permitted by the JHU equivalency formula.

Responsibilities

• Assist Principal Investigator or senior staff to ensure feasibility of protocol/study design.
• Develop standard operating procedures and data collection forms from protocols.
• Develop consent forms for clinical trials based on protocols.
• Prepare materials for IRB submission.
• Contribute to budget planning and resource allocation.
• Ensure compliance with protocols, procedures, and regulations.
• Develop and oversee recruitment strategies for participants.
• Set up data collection systems and ensure data validity.
• Organize and quality control study data.
• Participate in meetings and provide status updates.
• Conduct literature searches to provide background information.
• Abstract and index information according to subject matter knowledge.

Skills

Budget Management

Clinical Research Recruitment

Clinical Study Design

Clinical Trial Management System

Data Management and Analysis

Data Collection and Reporting

Good Clinical Practices

Interpersonal Skills

Project Management

Regulatory Compliance

Report Writing

Education

Bachelor's Degree in a related field

Job description

The Johns Hopkins University in Baltimore is seeking a Sr. Clinical Research Coordinator to oversee day-to-day operations of complex clinical studies, coordinating protocol activities, data collection, budgets, and regulatory compliance.

You will lead recruitment efforts, develop SOPs, prepare materials for IRB submission, collaborate with investigators across sites, and ensure data integrity and study milestones are met at Johns Hopkins Bayview.