Memory & Aging Research Nurse Coordinator

Washington University in St. Louis; Park (KS); On-site; USD 65,000 - 110,000; Full time

Benefits offered by this job

Vacation & holidays

Health insurance

Transit benefit (U-Pass)

Tuition assistance

Job summary

Washington University in St. Louis seeks a Memory and Aging Project Research Nurse Coordinator II to guide nurses and staff in long-term Alzheimer’s research.

You will collect health histories, administer cognitive assessments, and coordinate regulatory duties within a multidisciplinary team. Responsibilities include study start-up tasks, subject enrollment, and ensuring protocol adherence, with oversight of study medications and data quality.

Qualifications

• RN degree or diploma with active nursing license.
• Experience in clinical research coordination is preferred.
• Familiarity with IRB/HRO regulatory processes is beneficial.

Responsibilities

• Provide direct patient care and data collection for longitudinal dementia research.
• Identify, screen and enroll study subjects in coordination with the PI.
• Assist with IRB submissions, study start-up activities and regulatory documentation.
• Ensure protocol compliance and maintain source documentation across trials.
• Train and supervise study staff; oversee study medications and interventions.

Skills

Active Listening

Clinical Research Coordination

Clinical Research Management

Clinical Research Methods

Clinical Research Operations

Clinical Techniques

Database Management

Detail-Oriented

Effective Written Communication

Electronic Health Records (EHR)

Nursing Fundamentals

Oral Communications

Patient Recruitment

Reporting Tools

Spreadsheet Software

SAS

Team Collaboration

Education

Associate Degree In Nursing Or Diploma In Registered Nursing

Tools

SAS

Job description

Washington University in St. Louis seeks a Memory and Aging Project Research Nurse Coordinator II to guide nurses and staff in long-term Alzheimer’s research.

You will collect health histories, administer cognitive assessments, and coordinate regulatory duties within a multidisciplinary team. Responsibilities include study start-up tasks, subject enrollment, and ensuring protocol adherence, with oversight of study medications and data quality.