RN Clinical Research Coordinator

2 weeks ago


La Crosse, United States Gundersen Health System Full time

JOB REQUIREMENTS: Love + medicine is who we are, it\'s what we do, it\'s why people want to work here. If you\'re looking for a job to love, apply today. Schedule Weekly Hours:36 Gundersen Health System is seeking a full-time RN, Clinical Research Coordinator (RN-CRC) for our Clinical Research team working primarily in Hematology/Oncology. This is your opportunity to do the work you love in the of La Crosse, Wisconsin. What you will do: 0.9 FTE - 72 hours every two weeks 8 hours day shifts between 8am-5pm Monday-Friday Preform nursing assessments to monitor subject\'s progress during clinical research trials Support patient care coordination in relation to research Implement research protocols which may include administering investigational medication while utilizing the nursing process Facilitate scheduling of tests/procedures & collection/processing/submission of lab specimens What you will get: Stable hours, strong team support, and meaningful work. Support for your career growth through Professional Development Opportunities, our Tuition Reimbursement Program, and the Career Development Center Have your voice heard through our Nursing Shared Governance Councils Top-rated retirement plan and healthcare benefits What you will need: Associate degree or Bachelor\'s degree Nursing RN license to work in Wisconsin upon hire BLS for health care providers Minimum of 3 years RN experience Valid driver\'s license Gundersen Health System Hospital and Clinics comprises 7 hospitals and 33 clinics. We bring care close to home for our patients in Wisconsin, Minnesota, and Iowa. Inside our walls and our neighborhoods, we deliver world-class medical care and the right amount of love. We call it love + medicine and it\'s more than our practice. It is who we are.Job Description: The RN-Clinical Research Coordinator (RN-CRC) functions within the full scope of nursing practice, which includes being responsible for the process of patient identification, assessment, planning, implementation, monitoring, evaluation and coordination of care to meet the patient\'s health care needs in collaboration with health team members to ensure safe, quality care during the patient\'s entire course of participation in a clinical research trial. The RN-CRC meets the expectations of a professional employee. Major Responsibilities: 1. Performs nursing assessments, direct patient care, and monitors subject progress during the clinical trial, documenting medical data in subject study chart and in medical record. 2. Obtains and accurately documents structured subject medical, surgical and medication history. 3. Reviews Study Specific Trainings and applicable protocols for a thorough understanding of the study procedures, as they apply to their role and ensures that Delegation of Authority/Training Log for each study is completed in a proper and timely manner. 4. Performs informed consent... For full info follow application link. EEO/AA/Veterans/Disabilities ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/FC2DBFDBF71E4ABF



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