Clinical Research Nurse - Internal Medicine
About The Position
Founded in 1818, Saint Louis University is one of the nation’s oldest and most prestigious Catholic universities. SLU, which also has a campus in Madrid, Spain, is recognized for world-class academics, life-changing research, compassionate health care, and a strong commitment to faith and service. The Clinical Research Nurse I is responsible to carry out all delegated tasks related to complex protocols testing investigational drugs, devices, or research interventions. The Clinical Research Nurse I is a member of the team and resource for study protocol conduct acting as a liaison between the SLU SOM (School of Medicine), clinical partners (ex. SSM Health), the Principal Investigator, Institutional Review Board (IRB), and sponsors to ensure good clinical practice standards (GCP) throughout the life cycle of the study.
Requirements
- RN with current registration to practice nursing in St. Louis
- Three or more years of relevant nursing experience
- Current BLS Certification
Nice To Haves
- Clinical Research experience
Responsibilities
- Reviews and abstracts medical record information and ensures proper adherence to randomization schema, study drug dosing and administration
- Screens patients according to study criteria, randomize, enroll, and obtain consent
- Schedules, performs, and/or supervises required study tests
- Performs nursing assessments of study participants
- Documents and records, in writing or electronically, all study events and protocol related procedures
- Reviews clinical system billing charges for accuracy and appropriateness
- Ensures that all required study event(s) and protocol related data are accurately and efficiently entered in the clinical trial management system
- Applies knowledge of regulatory and institutional policies and processes appropriately in study documentation, protocol submissions, and standard operating procedures (SOPs)
- Enters and collects study related data and develops per appropriate processes; ensures accuracy and completeness of data for all studies; recognizes and reports security of physical and electronic data vulnerabilities
- Maintains participant-level documentation for all studies, including those that are complex in nature, require access to the EHR or require SLUCare/SSM charge routing; screens participants for complex studies (e.g., procedural, and interventional studies)
- Conducts visits for complex studies (e.g., procedural, and interventional studies)
- Identifies all adverse events (AEs) and determines whether or not they are reportable; collaborates with the PI to determine AE attributes, including relatedness to study; conducts and documents consent for participants for all types of studies, including those that are complex in nature and/or require clinical research orders in EHR
- Performs other duties as assigned
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
