Slu
Clinical Research Nurse - Internal Medicine
SLU Saint Louis, MO
Sponsorship not specifiedDetected 14 days ago
GCPHREHR/EMRClinical TrialsClinical ResearchResearchCommunicationMicrosoft OfficeGxP
About the role
- The Clinical Research Nurse I is responsible to carry out all delegated tasks related to complex protocols testing investigational drugs, devices, or research interventions.
- 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.
- Reviews and abstracts medical record information and ensures proper adherence to randomization schema, study drug dosing and administration
Responsibilities
- Performs nursing assessments of study participants
- Documents and records, in writing or electronically, all study events and protocol related procedures
- 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)
- 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
Requirements
- Schedules, performs, and/or supervises required study tests
- 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)
Nice to have
- Clinical Research experience
- Clinical Research
- Scheduled Weekly Hours:
- Saint Louis University is an equal opportunity/affirmative action employer.
- If accommodations are needed for completing the application and/or with the interviewing process, please contact Human Resources at 314-977-5847.
Skills
- Knowledgeable in regulatory and institutional policies and processes
- Proficiency in electronic medical records and relevant computer software
- Strong verbal and written communication skills and attention to detail
- Ability to use computing software and web based applications (e.g., Microsoft Office products and the electronic medical record)
- Ability to work in a team environment to facilitate the integrity of the study and its timely completion
- Ability to travel to off-site locations
Benefits
- 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.
Company info
- Founded in 1818, Saint Louis University is one of the nation's oldest and most prestigious Catholic universities.
Equal opportunity
- equal opportunity/affirmative action employer.
This listing is sourced directly from Slu's careers page and normalized into a canonical job model.