Clinical Research Nurse Coordinator I

Washington University in St. Louis; St. Louis (MO); On-site; USD 60,000 - 100,000; Full time

Benefits offered by this job

Vacation and holidays

Health insurance

Transit pass

Tuition assistance

Caregiver leave

Job summary

Washington University in St. Louis seeks a Research Nurse Coordinator to support coordination and implementation of research studies, data collection, and data management within study protocols.

You will work with multidisciplinary teams to ensure patient safety and data integrity, under the PI's guidance. Responsibilities include assisting with IRB submissions, enrolling participants, coordinating procedures, and ensuring compliance with regulations.

Qualifications

• Graduate of an accredited nursing program.
• Current RN licensure in Missouri and/or Illinois depending on location.
• B.S.N. - Bachelor of Science in Nursing preferred.

Responsibilities

• Works under PI guidance to meet research objectives.
• Assists with IRB applications and continuing reviews.
• Provides direct patient care, including assessment, planning and evaluation.
• Identifies, screens and enrolls study subjects.
• Ensures protocol requirements are met and coordinates study procedures.
• Prepares and submits reportable event reports to sponsor, IRB and regulators.
• Collaborates with sponsor research associates during monitoring activities.
• Administers investigational products in approved settings.
• Educates staff nurses about the study and procedures.

Skills

Clinical Research

Nursing Fundamentals

Database Management

Electronic Health Records

Team Collaboration

Critical Thinking

Interpersonal Relationships

Spreadsheet Software

Statistical Analysis Software

Oral Communications

Effective Written Communication

Patient Recruitment

Education

Bachelor of Science in Nursing

RN licensure MO/IL

Job description

Washington University in St. Louis seeks a Research Nurse Coordinator to support coordination and implementation of research studies, data collection, and data management within study protocols.

You will work with multidisciplinary teams to ensure patient safety and data integrity, under the PI's guidance. Responsibilities include assisting with IRB submissions, enrolling participants, coordinating procedures, and ensuring compliance with regulations.