Job Description

Clinical Research Nurse II- ICON- Salt Lake City UT ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Nurse II to join our diverse and dynamic team. As a Clinical Research Nurse II at ICON, you will play a pivotal role in the planning, implementation, and coordination of clinical research studies, ensuring adherence to protocol requirements and ethical standards, while contributing to the advancement of medical science and patient care. **Title:** Clinical Research Nurse II **Job Type** : Full Time/Permanent **Shift/Schedule:** 10 hour shifts, 4 x/week + Must have availability M-F 7 AM-5 PM + Must have flexibility for at least 2 weekends each month if needed (if you are scheduled for a weekend shift, you wouldn't work during the week). **Location:** 100% on site Salt Lake City UT **What you will be doing** + Collaborating with study investigators and multidisciplinary teams to develop and execute clinical research protocols, including participant recruitment, enrollment, and follow-up visits, in accordance with regulatory guidelines and standard operating procedures (SOPs). + Conducting comprehensive patient assessments, administering study treatments and interventions, and monitoring participant safety and well-being throughout the duration of the study, while documenting all clinical observations and study-related procedures accurately and efficiently. + Collecting, recording, and analyzing clinical data, including vital signs, laboratory results, and adverse events, in electronic case report forms (eCRFs) and study databases, while ensuring data integrity and compliance with Good Clinical Practice (GCP) standards. + Providing education and support to study participants and their families regarding study procedures, treatment protocols, and informed consent, while addressing any questions or concerns and ensuring adherence to study requirements and timelines. + Collaborating with regulatory agencies, ethics committees, and institutional review boards (IRBs) to obtain study approvals, maintain regulatory compliance, and ensure the ethical conduct of clinical research studies, while upholding patient confidentiality and privacy rights. **Your profile** + Bachelor's degree in Nursing (BSN) from an accredited institution, with current licensure as a Registered Nurse (RN) in the applicable jurisdiction. + Minimum of 2+ years of clinical nursing experience, preferably in a research or academic healthcare setting, with demonstrated knowledge of clinical trial operations, GCP guidelines, and regulatory requirements governing human subjects research. + Strong clinical assessment and critical thinking skills, with the ability to independently manage study protocols, prioritize tasks, and make informed decisions in a fast-paced, dynamic environment, while ensuring patient safety and protocol compliance. + Excellent communication and interpersonal skills, with the ability to effectively collaborate with diverse stakeholders, including study investigators, research coordinators, and study participants, while maintaining professionalism and integrity in all interactions. + Proficiency in electronic medical record (EMR) systems, data management tools, and Microsoft Office applications, with a high level of attention to detail and accuracy in documenting patient information and study data. **What ICON can offer you:** Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: + Various annual leave entitlements + A range of health insurance offerings to suit you and your family's needs. + Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. + Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. + Life assurance + Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site ( to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here ( to apply

Job Tags

Permanent employment, Full time, Work at office, Flexible hours, Shift work, Weekend work,

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