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Registered Nurse/ Licensed Practical Nurse/RN/LPN

Infotree Service Inc

This is a Full-time position in Chicago, IL posted February 22, 2021.

Job DescriptionJOB TITLE: Research NurseLOCATION: North Chicago, ILDURATION: 12 MonthsMARKET PURPOSESupport study sites in the coordination of Phase I-IV clinical research studies, ensuring that studies are carried out according to protocol, standard operating procedures, GCP, and other applicable guidelines and regulations.RESPONSIBILITIESCoordinate clinical research studies conducted by a supervising principle investigator.Update and maintain skills, training and knowledge of current best nursing practice and topics related to clinical research.Safeguard the well-being of the subjects and ensure and maintain high standards:Maintain a safe environment in accordance with the Health and Safety policies;Act as volunteer advocateDeal with volunteer and visitor concerns in a pro-active manner and taking remedial action as required;Assist staff, both registered and unregistered in Nursing Practices and the delivery of care to the volunteer;Report any deviation from normal practice to senior staff.Support study conduct by:Review of the study protocol, case report form (CRF), other study documents, and electronic data capture systems;oParticipate in project meetings with the project team as needed;Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, setting up equipment and documents;Plan logistical activity for procedures as per protocol;Generate volunteer instructions;oIdentify and obtain required supplies and equipment;oPrepare and deliver study specific training materials, documents, and records;oTroubleshoot study issues;Participate in huddles to ensure daily tasks are assigned to team members are executed to the expected standards;Assist with data quality checking and query resolution to ensure that data collected on study volunteers adhere to study protocol and ensuring quality control for content accuracy and completeness.Recruit and Screen volunteers for inclusion in study based on pre-determined criteria.Orientate volunteers to the study and the site including the purpose of the study, procedures and practical issues such as timelines for visits.Responsible for the correct administration and custody of study drug according to site standard operating procedures.Perform a variety of complex clinical procedures on subjects including but not limited to ECG, sample collection including phlebotomy, spirometry, vital signs, cannulation, and cardiac telemetry monitoring.Collect, record, and report clinical data and findings appropriately in case report forms (CRFs).Collaborate closely with study investigator informing on relevant adverse events and serious adverse events according to procedures outlined in the protocol.Cooperate with study monitor and reserve sufficient time for questions during monitoringQualificationsEQUIRED KNOWLEDGE, SKILLS AND ABILITIESGood knowledge of clinical trialsIn-depth knowledge of the principles of Good Clinical Practices (GCP)Good skill in using MS Windows and Office applicationsEffective written and verbal communication skills including good command of the English languageExcellent interpersonal skillsExcellent problem-solving skillsEffective organizational skillsAbility to pay close attention to detailAbility to establish and maintain effective working relationships with coworkers, managers and clientsMINIMUM REQUIRED EDUCATION AND EXPERIENCEBachelor’s degree or educational equivalent in Nursing and 1 year relevant experience; or equivalent combination of education, training and experienceCurrent active nursing license in the state, country, or region in which the site residesApplicable certifications and licenses as required by company, country, state, and/or other regulatory bodiesPHYSICAL REQUIREMENTSUse of telephone and face-to-face communication requiring accurate perception of speechUse of keyboard requiring repetitive motion of fingersFrequent mobilization around the facilityAdditional InformationAll your information will be kept confidential according to EEO guidelines.

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