Registered Nurse

Registered NurseHonorVet Technologies is a Service-Disabled Veteran-Owned IT staffing firm, ISO 9001 and ISO 27001 certified, working with federal agencies, state governments, and Fortune 500 enterprise clients across the US. What makes us different isn't a tagline; it's the way we work. We don't forward resumes and hope for the best. We take the time to understand where a professional like you are headed and only reach out when we genuinely believe there's a fit worth exploring.Job Title: Registered Nurse Location: Chicago, IL 60637 (Onsite) Duration: 3 Months Part Time: 3-4 days per week Working hours: 24-32 hours per week (Hours can be discussed during interview, typical hours 8am-2pm or 8am-4pm)Job Description: Under the direction of the Principal Investigator (PI), Co-Investigators, and Research Manager (RM), the Clinical Research Nurse facilitates the daily activities of complex clinical trials and plays a critical role in the conduct of the studies to ensure compliance with federal and institutional regulations. The Clinical Research Nurse provided clinical expertise within the department/unit through improving clinical research practice and serving as a resource to others. Additionally, the Clinical Research Nurse works with the PI, department, sponsor, and institution to support and provide guidance on the administration of compliance, financial, personnel, and other related aspects of clinical studies.Key Responsibilities: • Coordinate and participate in the conduct of clinical research trials at the Institute. • Assist with or plan and implement the clinical study's goals and objectives; organize patient enrollment planning; conduct quality assurance activities, compile and analyze data. • Develop and implement study procedures, maintains study records, tracks study progress, and conducts quality assurance on study data collected. • Act as a liaison with medical staff, university departments, ancillary departments and/or satellite facilities. • Conduct clinical study tasks including physical assessment of subjects, taking vital signs, recording medical, surgical, social and behavioral histories, and phlebotomy skills. • Serve as a resource person or act as a consultant within area of clinical expertise. • Act as a leader within the department/unit through improving clinical research practice and serving as a resource. • Maintain working knowledge of current protocols, and internal SOPs. • Be accountable for high standards of clinical research practice and assist in the development of accountability in others. • Oversee and participate in the coordination and conduct of complex clinical research studies and ensure compliance with study standard operating protocols and procedures as well as federal and institutional regulations. • Provide Investigators with guidance regarding protocol requirements. • Maintain regulatory documentation. • Assist other research personnel with reports to regulatory agencies, such as the IRB, FDA and Data and Safety Review Committee. • Prepare for and assist with audits, inspections, and monitoring visits from regulatory agencies or sponsors. • Applies logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems. • Performs other related work as needed.Required Education: • Bachelor of Science in Nursing required Required Experience: • Phlebotomy and intravenous line placement experience preferred. • Clinical research experience preferred. • Experience with Epic or other electronic medical records preferredRequired Licenses and Certifications: • Current valid Registered Nurse – Illinois license required.Required Technical Knowledge or Skills: • Demonstrated ability to access computer programs and use or learn basic computer operations. • Fundamental working knowledge of clinical research. • Knowledge of patient care fundamentals, including aseptic principles and techniques. • Ability to provide direct patient care in a professional and respectful manner. • Ability to read medical documents and instruments. • Ability to participate in protocol review and clinical trials evaluations. • Excellent interpersonal skills. • Excellent verbal and written communication. • Strong data management skills and attention to detail. • Excellent time management and ability to prioritize work assignments. • Ability to read, understand, and implement clinical trials protocols. • Working knowledge of Good Clinical Practices (GCP). • Working knowledge of Microsoft Word, Excel and Adobe Acrobat.Unit Working Conditions: • Office and clinic • Occasional weekend/evening hours for enrollment events at community partner locations. • Travel may be required for enrollment events at community partner locations.Application Documents: • Resume (required) • Cover Letter (preferred)