ALS Trials Lead — Clinical Research Coordinator

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

Job summary

Johns Hopkins University is seeking a Sr. Clinical Research Coordinator to oversee day-to-day activities of interventional studies investigating ALS. You will lead regulatory and data processes, develop recruitment strategies, and collaborate with sponsors and investigators to ensure protocol adherence.

The role requires preparing SOPs, consent forms, and IRB materials, while managing budgets and data systems. This is a full-time position in the School of Medicine Campus with exempt status.

Qualifications

• Bachelor's degree in a related field.
• Three years of related experience required; additional education may substitute for experience.
• Master's degree in a related field preferred.

Responsibilities

• Assist PI and senior staff to ensure feasibility of protocol/design.
• Develop SOPs and data collection forms from protocols.
• Create consent forms for clinical trials.
• Prepare IRB submissions and regulatory documents.
• Collaborate with sponsors to assess resources and costs.
• Ensure compliance with protocols and regulations.
• Contribute to study budget development.
• Develop participant recruitment strategies and data capture systems.
• Setup data collection systems and ensure data quality.
• Audit study data and participate in meetings to propose protocol improvements.
• Conduct literature searches and index information for studies.

Skills

Budget Management

Clinical Research Recruitment

Clinical Study Design

Clinical Trial Management System

Data Management

Data Collection

Good Clinical Practices

Interpersonal Skills

Project Management

Regulatory Compliance

Report Writing

Education

Bachelor's Degree in a related field

Three years of related experience

Master's Degree preferred

Job description

Johns Hopkins University is seeking a Sr. Clinical Research Coordinator to oversee day-to-day activities of interventional studies investigating ALS. You will lead regulatory and data processes, develop recruitment strategies, and collaborate with sponsors and investigators to ensure protocol adherence.

The role requires preparing SOPs, consent forms, and IRB materials, while managing budgets and data systems. This is a full-time position in the School of Medicine Campus with exempt status.