Research Nurse Coordinator for Clinical Trials

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

Benefits offered by this job

Tuition assistance for family

Caregiver leave – 4 weeks

Metro transit U-Pass

Job summary

Washington University in St. Louis is seeking a Clinical Research professional to coordinate and implement research study activities, collect data, and manage data generated by study protocols. You will work with multidisciplinary teams to ensure patient care, regulatory compliance, and data integrity.

The role involves assisting with IRB submissions, protocol adherence, and coordination of study procedures, with opportunities to educate staff and oversee study medications as appropriate.

Qualifications

• Nursing degree or diploma; BSN preferred.
• Current RN licensure in MO and/or IL.
• Experience in clinical research coordination preferred.
• Knowledge of regulatory requirements and source documentation.

Responsibilities

• Coordinate with PI to meet project objectives.
• Assist with start-up activities including IRB applications and amendments.
• Provide direct patient care, collect data, and assist physicians.
• Identify, screen and enroll study subjects.
• Ensure protocol requirements are met and manage data entry.

Skills

Clinical Research

Clinical Research Coordination

Clinical Research Management

Clinical Research Methods

Clinical Research Operations

Nursing Fundamentals

Critical Thinking

Database Management

EHR

Interpersonal Relationships

Oral Communications

Patient Recruitment

Spreadsheet Software

SAS

Team Collaboration

Education

Bachelor of Science in Nursing (BSN)

RN Licensure in MO/IL

Tools

SAS

EHR

Spreadsheet Software

Job description

Washington University in St. Louis is seeking a Clinical Research professional to coordinate and implement research study activities, collect data, and manage data generated by study protocols. You will work with multidisciplinary teams to ensure patient care, regulatory compliance, and data integrity.

The role involves assisting with IRB submissions, protocol adherence, and coordination of study procedures, with opportunities to educate staff and oversee study medications as appropriate.