Clinical Research Nurse Coordinator I

Washington University in St. Louis; St. Louis (MO); On-site; USD 60,000 - 99,900; Full time

Benefits offered by this job

Vacation & holidays

Metro U-Pass

Tuition assistance

Job summary

Washington University in St. Louis is seeking an RN Research Nurse Coordinator I to support the Center for Clinical Studies.

You will coordinate data collection, assist with study start-up, enroll participants, and ensure protocol and regulatory compliance while safeguarding human subjects. You will work with multidisciplinary teams, educate staff, manage source documents, and help maintain study integrity in a busy on-campus environment.

Qualifications

• Graduate of an accredited nursing program.
• Current RN licensure in MO and/or IL per location.
• Basic Life Support certification (BLS) from recognized providers.

Responsibilities

• Coordinate with PI and study team to meet research objectives.
• Assist with study start-up activities including IRB submissions and amendments.
• Provide direct patient care, document data, and assist physicians.
• Identify, screen, and enroll study subjects.
• Ensure protocol requirements and regulatory compliance are met.
• Coordinate specimen handling and data entry; maintain source documents.
• Submit reportable event reports to sponsors/IRB/regulators.
• Educate nursing staff on study procedures and potential adverse events.

Skills

Clinical Research

Clinical Research Coordination

Clinical Research Management

Clinical Research Methods

Clinical Techniques

Critical Thinking

Database Management

Electronic Health Records

Interpersonal Relationships

Nursing Fundamentals

Oral Communications

Patient Recruitment

Spreadsheet Software

SAS

EHR Systems

Education

Graduate of an accredited nursing program

BSN/Bachelor of Science in Nursing

Tools

SAS

Electronic Health Records (EHR)

Job description

Washington University in St. Louis is seeking an RN Research Nurse Coordinator I to support the Center for Clinical Studies.

You will coordinate data collection, assist with study start-up, enroll participants, and ensure protocol and regulatory compliance while safeguarding human subjects. You will work with multidisciplinary teams, educate staff, manage source documents, and help maintain study integrity in a busy on-campus environment.