Clinical Research Nurse

Saint Louis University School of Medicine Departments withCurrent Opportunities: Internal Medicine, Cancer Center, or Neurology

Join Our Clinical Research Team

Saint Louis University (SLU) School of Medicine is seeking experienced and compassionate Registered Nurses to contribute directly to SLU's research enterprise by supporting innovative clinical trials and research studies that advance knowledge, improve treatments, and ultimately impact patients.

As a Clinical Research Nurse, you willworkalongside physicians/principal investigators tocoordinate and conduct clinical research activities for studies involving investigational drugs, medical devices, procedures, and other research interventions. The Clinical Research Nurse serves as a key liaison between research participants, investigators, sponsors, institutional review boards, and clinical partners to ensure studies are conducted in accordance with Good Clinical Practice (GCP), regulatory requirements, and institutional policies.

These positions combine clinical nursing expertise, patient advocacy, research coordination, and regulatory compliance to support a broad portfolio of clinical trials.

Why Join Saint Louis University?

• Monday-Friday schedule, (5 - 8 Hour Shifts/week)

• Flexible work schedules available based on department needs

• 15 vacation days, 13 sick days, 10+ paid holidays each year

• Tuition remission for employees and eligible dependents

• Comprehensive medical, dental, vision, and retirement benefits

• Collaborative environment with opportunities for professional growth and development

• Saint Louis University offers the opportunity to combine patient care with scientific advancement while enjoying a strong work-life balance and exceptional benefits.

Key Responsibilities

• Screen, recruit, consent, enroll, and retain research participants according to study protocols.

• Conduct nursing assessments and monitor participants throughout study participation.

• Coordinate and manage study visits, procedures, testing, and follow-up activities.

• Review medical records and collect relevant clinical data for research studies.

• Administer and monitor investigational therapies and study-related interventions as permitted by protocol.

• Document study activities, participant interactions, and protocol-related procedures in electronic systems and source documentation.

• Ensure accurate and timely entry of study data into clinical trial management systems and sponsor databases.

• Collaborate with investigators, research coordinators, sponsors, and clinical partners to maintain protocol compliance.

• Monitor, identify, document, and report adverse events and protocol deviations.

• Support regulatory submissions, study audits, monitoring visits, and compliance activities.

• Maintain participant confidentiality and ensure the integrity and security of research data.

• Apply institutional, federal, and regulatory requirements governing human subjects research.

• Serve as a resource for research participants and interdisciplinary study teams.

• Perform additional duties as assigned.

Knowledge, Skills, and Abilities

• Knowledge of clinical nursing practices and patient care standards.

• Strong organizational, documentation, and time management skills.

• Ability to manage multiple studies and competing priorities in a fast-paced research environment.

• Excellent verbal and written communication skills.

• Strong attention to detail and commitment to regulatory compliance.

• Proficiency with electronic medical records (EMR/EHR), Microsoft Office, and clinical research software systems.

• Ability to work independently and collaboratively within multidisciplinary teams.

• Ability to travel to off-site clinical or research locations as needed.

Minimum Qualifications

• Registered Nurse (RN) with current Missouri nursing license or eligibility for Missouri licensure.

• Current Basic Life Support (BLS) certification.

• Three (3) years of professional nursing experience.

• Proficiency with electronic medical records and Microsoft Office applications.

Preferred Qualifications

• Clinical research experience

• Experience working within an academic medical center, hospital, or healthcare research setting.

Apply today to join a mission-driven team to improve lives through research.