Critical Care RN - Research Team (Clinical Trials) - 80& travel {168634}

Are you a passionate Critical Care/Acute Care nurse looking to take your talents to the next level? Join us and leverage your expertise to support cutting-edge research on-site at hospitals across the US! You'll be the face of our BD/APM monitoring portfolio, providing essential education and training to nurses and doctors in hospital ICUs and operating rooms. With 80% travel, every day will bring new challenges and opportunities to make a difference! Enjoy comprehensive on-the-job training to master clinical trial implementation and good clinical practices, along with our advanced monitoring platforms and disposables. This is your chance to impact patient care without direct hands-on responsibility—your role will be all about empowering medical professionals with your knowledge. Critical Information Can be up to 40hours per week- some weeks 10-20 hours. 3 years of experience needed Education/Licenses Needed Discover the qualifications you need to elevate your career—check with a Recruiter or Staffing Manager! Benefits: • Enjoy a generous benefits package available to full-time employees after just 90 days! • Secure your future with a 401(k) that includes a company match after 1 year of service! Provide research interventions to clinical research patients Managing clinical research studies activities Perform clinical research and coordinate research activities Ascertaining patient eligibility for clinical trials Promote research study initiation and review Manage the clinical research programs and activities Determining eligibility of patients for clinical trials Coordinate research programs that integrate new advances in clinical trials Participate in the development of clinical research protocols Maintain research databases and related records needed for research Maintain and organize research study supplies and prepare study kits Meet study timelines and research participant schedule Participate in clinical research studies conducted by a supervising investigator Supervise or manage other research staff (clinical research coordinators and/or data coordinators) Maintaining records for patients enrolled in clinical trials Act as patient advocate in managing clinical trials Perform clinical research and patient treatment in conjunction with a specified clinical research protocol(s) Verify patient eligibility for clinical investigative studies Using protocol inclusion/exclusion criteria Explain study to patients and potential patients