RN, Research

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.

Job Location (Full Address):

220 Hutchison Rd, Rochester, New York, United States of America, 14620

Opening:

Worker Subtype:

Regular

Time Type:

Full time

Scheduled Weekly Hours:

40

Department:

400048 Medicine M&D-Infect Dis Unit

Work Shift:

Range:

UR URC 212 H

Compensation Range:

$30.33 - $42.47

The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.

Responsibilities:

Participate in ongoing research studies in the Vaccine Research Unit relating to respiratory illnesses such as influenza and COVID-19, phase 1-3 vaccine studies, studies in therapeutic agents in both adults and pediatric populations. Position requires the ability to work independently, strong interpersonal skills in communicating with adult subjects and their families, their health care providers, and hospital staff at Strong, Highland and RGH, and a willingness to develop the logistics of subject enrollment, persistence and flexibility in assuring on-going subject cooperation and good data collection skills. On occasion, this position may require travel to private medical offices and Urgent Care facilities in the Rochester area to enroll potential subjects and obtaining required samples.

Responsibilities GENERAL PURPOSE: This position is for a Research nurse for the AIDS Clinical Trials Group (ACTG) clinical research site within the division of Infectious Diseases. Studies currently being conducted include long-term observational studies, therapeutic vaccine, and therapeutic agents in persons living with HIV. Applicants should be able to work with a variety of participants and have clinical nursing skills as well as clinical research experience. The research nurse will work under general direction and with latitude for independent judgment to assume full responsibility for various clinical projects as outlined below. RESPONSIBILITIES: Human Subject Recruitment: Identification of participant pools via electronic medical record review and discussion with clinical team members. Review of upcoming clinic schedule to identify potential participants coming into clinic. Determination of eligibility and screening in clinic setting and/or over the telephone. Obtain informed consent and performance of enrollment procedures. Ability to communicate effectively with participants to answer questions and ensuring they understand the clinical study and their involvement. Assist with providing outreach to study participants to maximize their retention in a project. Collaborate with community stakeholders to increase awareness about variety of research projects. May attend the Community Advisory Board Meetings or community events as needed. Clinical Study Visits and Clinical Assessments: Conducts unstructured interviews with participants, as well as administer all protocol required study procedures on participants. These can include but are not limited to venipuncture, peripheral IV insertion and infusion of medications, intramuscular injections, collection of vital signs and various other specimens (e.g., oral rinses, vaginal swabs, and urine samples), neuropsychological testing, point-of-care testing and ECGs. Measure, record, interpret, and report indicators of health status. Evaluate for local or systemic reactions to determine adverse events to study treatments for protocol required reporting. Research Team Collaboration: Attend and participate in weekly team meetings and monthly research group or clinic meetings. Participation in unique protocol or sponsor-required trainings prior to study start. Establish and maintain relationships with sponsor and protocol representatives for the purpose of regulatory compliance and quality assurance/control. Regularly communicate with investigational drug pharmacy and laboratory staff with regard to study visit coordination and study treatment requirements. Quality Assurance/Control: Develop, implement, and perform QA/QC measures to optimize site study performance. Collaborate on the development and implementation of site standard operating procedures and site-specific procedures to ensure standardization of