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AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Clinical Research Nurse

Lake County, Illinois Req ID 2204689 Category Research and Development Division AbbVie

*This position will be majority 3rd shift but if need arises, will pull to 2nd shift too. Work schedule will be 24 hours per week, 12 hours Friday and 12 hours Saturday.*

The Clinical Research Nurse is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). Assists with the execution of study-related activities of a Phase I clinical research study. Research nurses should primarily be concerned with the protection and care of research subjects. The primary role is to function as a licensed registered nurse engaged in the practice of care/assessments of the healthy volunteers and/or patient. Position includes disseminating information regarding new information for documentation, performance improvement and data source upgrades.

•Review protocols and informed consent forms for scheduled studies, identify and communicate potential issues to the appropriate personnel. •Participate in nursing study related activities as required by protocol compliance with Corporate, divisional, and departmental SOP’s and external (CFR, ICH GCP) regulatory guidelines. Responsible for compliance with applicable Corporate and Divisional Policies and Procedures. •Evaluate adverse events and manage safety reporting activities in a timely manner. •Interact with the Principal Investigator and other study physicians, Recruiting/Screening, Data Systems, and other personnel in support of study-specific activities. •Support quality and compliance improvement initiatives as appropriate. •Participate in the recruitment and screening activities to ensure successful enrollment of volunteers into studies scheduled at the Phase 1 Unit. Interfaces with research participants to support efforts to determine eligibility and consenting of study participants according to protocol. Review and assess data collected. Serve as a resource person or act as a consultant within area of clinical expertise (R/S). •Disburses investigational drug and provides teaching regarding administration, as necessary. Develops accurate source materials and ensures compliance from site staff. Ensures all protocol procedures are completed per study requirements (Unit).


•For Recruiting & Screening: Minimum of a diploma from an accredited nursing school and 1-3 years work experience in a clinical research environment For Unit: Bachelor of Nursing or other Science degree preferred with 1-3 years of nursing experience in a hospital setting; and/or ER/ICU experience •Nursing competency skills per scope of practice (i.e., performing vital signs, nursing assessments, performing ECG/EKG, administering injections, etc.) •Fundamental working knowledge of clinical research •Advanced Life Support and Cardio-Pulmonary Resuscitation within six months •Ability to organize and prioritize responsibilities while paying close attention to detail

Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel: No
Job Type: Experienced
Schedule: Part-time

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