Under the direction of the Associate Director and Principal Investigator or designee, 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, 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. Primary responsibilities include reviewing and abstracting medical record information, ensuring adherence to randomization schema, study drug dosing and administration, screening patients according to study criteria, randomizing, enrolling, and obtaining consent, scheduling and supervising required study tests, performing nursing assessments, documenting all study events and protocol related procedures, reviewing clinical system billing charges, ensuring accurate data entry in clinical trial management systems, applying regulatory and institutional policies, maintaining participant-level documentation, conducting visits for complex studies, identifying and reporting adverse events, and performing other duties as assigned. Knowledge, skills, and abilities required include proficiency in electronic medical records and relevant software, strong communication skills, attention to detail, ability to work in a team, and ability to travel to off-site locations. Minimum qualifications include RN registration in St. Louis, 3-5 years nursing experience preferably in Oncology, current BLS certification, and computing software proficiency. Clinical research experience is strongly preferred.
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