Clinical Research Associate (CRA), II University of UtahClinical Research Associate (CRA), IISalt Lake City, UT$65,000–$70,000 / yearFull timeThe Clinical and Translational Sciences Institute (CTSI) is seeking a highly motivated individual to join our team providing QA and compliance support for the Clinical Research Support Office (CRSO) ensuring continuity and increasing efficiencies between the different Departments and study teams. Works in collaboration with the Office of Research Integrity and Compliance, Huntsman Cancer Institute and Internal Medicine along with other Departments campus wide to develop campus-wide processes and procedures.
PS Sr Research Nurse University of UtahPS Sr Research NurseSalt Lake City, UT$60,700–$109,000 / yearFull timeOften: Infectious disease, oils (there is air or skin exposure to oils or other cutting fluids), hazards (includes a variety of physical conditions, such as proximity to moving mechanical parts, moving vehicles, electrical current, working on scaffolding and high places, or exposure to chemicals). Essential FunctionsServes as a neurovascular "nurse navigator" by coordinating referrals, patient/family education and care planning, relating to patients with neurovascular pathologies, streamlining their care experience at the University.
NewClinical Laboratory Scientist United States ArmyClinical Laboratory ScientistSalt Lake City, UTBenefits may include: ★ Repayment of qualified education loans to lending institution, paid annually over a maximum of three years while serving ★ Travel opportunities, to include humanitarian missions ★ Up to 30 days of paid vacation earned annually ★ Enrollment in a military retirement system that blends the traditional legacy retirement pension with a defined contribution to service members’ Thrift Savings Plan account ★ No- to low-cost medical and dental care for you and your family ★ Commissary and post exchange shopping privileges ★ Possible specialized training assistance and monthly stipend while enrolled in an accredited residency program ★ Specialized training to become a leader in medicine Eligibility Requirements ★ Must have a bachelor’s degree from a DA-approved accredited college or university ★ Must have a certification in Medical Technology/Medical Laboratory Science by the American Society for Clinical Pathology (ASCP) with one-year work experience ★ Must be a U.S. citizen for Active Duty ★ Must have a permanent U.S. residency to serve in the Army Reserve Have questions or want more information? Outstanding Benefits When you join the Army Medical Service Corps, you’ll be making a difference in the lives of our Soldiers and the country at large while gaining access to invaluable opportunities, like supporting humanitarian missions, leadership training and a competitive benefit package.
Clinical Research Associates (CRA) University of UtahClinical Research Associates (CRA)Salt Lake City, UT$65,000–$70,000 / yearVP Area U of U Health - Academics Department 02148 - Clinical Research Service Ofc Location Campus City Salt Lake City, UT Type of Recruitment External Posting Pay Rate Range $65,000-$70,000 Close Date 10/23/2026 Priority Review Date (Note - Posting may close at any time) Job Summary. Open Date 08/21/2026 Requisition Number PRN45975B Job Title Clinical Research Associates (CRA) Working Title Clinical Research Associate (CRA), II Career Progression Track P00 Track Level P2 - Developing FLSA Code Administrative Patient Sensitive Job Code?
NewVirtual CRA Info Session 11.4.2026 (Clinical Research Coordinator Experience) Medpace Holdings IncVirtual CRA Info Session 11.4.2026 (Clinical Research Coordinator Experience)Salt Lake City, UTConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and. Must have a minimum of a Bachelor's degree in a health or science related field; Experience as a Clinical Research Coordinator (minimum 2 years); Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely; Must maintain a valid driver's license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft Office; Strong communication and presentation skills; and.
Senior Clinical Research Associate - Psychiatry - West Coast (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Psychiatry - West Coast (Remote)UTRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Clinical Research Associate - Sponsor Dedicated IQVIA Holdings IncClinical Research Associate - Sponsor DedicatedSalt Lake City, UT$71,900–$189,000 / yearIn this role, you will be responsible for overseeing clinical trial sites to ensure studies are conducted in compliance with study protocols, regulatory requirements, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and sponsor expectations. Successful candidates will possess strong site management skills, a commitment to quality, and the ability to build productive relationships with investigators and site personnel.
West Coast Clinical Research Associate II ICON PlcWest Coast Clinical Research Associate IIUtah, UTICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
FSP Clinical Research Associate 2 - West Region Fortrea IncFSP Clinical Research Associate 2 - West RegionUTRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewFSP Clinical Research Associate 2 - West, Central, and South Regions Fortrea IncFSP Clinical Research Associate 2 - West, Central, and South RegionsUTRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
Clinical Research Associate II ICON PlcClinical Research Associate IISalt Lake City, UT$91,336–$114,170 / yearWilling and able to travel up to 50% for on-site monitoring visits across northwest region; preference given to candidates residing in Pacific NW, Utah, or Northern California near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceUTTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedUTTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Clinical Research Coordinators (Non-R.N.) University of UtahClinical Research Coordinators (Non-R.N.)Salt Lake City, UT$60,000–$85,000 / yearThe Senior Clinical Research Coordinator is a senior operational leader supporting a portfolio of multiple investigators and active protocols across University and VA research environments, serving as a REDCap and regulatory subject matter expert, mentoring research staff, and leading operational improvement initiatives. The Senior Clinical Research Coordinator provides advanced leadership and oversight of a complex portfolio of clinical, translational, and health services research studies within the Division of Geriatrics, independently managing studies across the University of Utah and VA Salt Lake City Health Care System.
Clinical Research Project Coordinator Intermountain Healthcare IncClinical Research Project CoordinatorMurray, UT$27.65–$43.55 / hourBased on role, may coordinate (1) review of IRB/HRPP submissions and provide support to research oversight committees and research programs, coordinate review and oversee submission, or (2) centralized administrative and technical functions associated with grants, contracts and other agreements from external funding sources. Responsibilities include negotiating budgets with external sponsors for industry-funded trials, as well as managing internal processes such as CTMS study builds, Medicare Coverage Analysis development and approval, and review of research-related patient charges to ensure compliance and financial accuracy.
Clinical Research Coordinator, On-Site, Bountiful, Utah IQVIAClinical Research Coordinator, On-Site, Bountiful, UtahBountiful, UtahJoin Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits.
PS Clinical Research Coord University of UtahPS Clinical Research CoordSalt Lake City, UT$39,300–$72,700 / yearThis position will: (1) assist in facilitating the conduct of clinical research by performing research duties for Vascular Surgeon Research Investigators; (2) coordinate technical and administrative details involved in both sponsor and physician-initiated clinical research studies; and (3) assist the Principal Investigator and study team in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures; and (4) coordinate clinical trials involving the investigational use of medical devices and drugs, including studies conducted under IDE and IND requirements. Full Time Shift Day Work Schedule Summary VP Area U of U Health - Academics Department 00917 - Vascular Surgery Development Location Campus City Salt Lake City, UT Type of Recruitment External Posting Pay Rate Range 39300 to 72700 Close Date 11/28/2026 Priority Review Date (Note - Posting may close at any time) Job Summary.
NewClinical Research Management University of UtahClinical Research ManagementSalt Lake City, UT$86,773–$106,901 / yearThis position manages research nursing, regulatory, and data management staff; oversees study startup, conduct, and closeout activities; ensures compliance with institutional and regulatory requirements; and collaborates with investigators, sponsors, and clinical partners to support a robust neonatal research portfolio. Open Date 09/11/2026 Requisition Number PRN46194B Job Title Clinical Research Management Working Title Research Nurse Manager Career Progression Track M00 Track Level M4 - Senior Manager, M3 - Manager, M2 - Senior Supervisor FLSA Code Administrative Patient Sensitive Job Code?
Clinical Research RN (Day Shifts) CenExelClinical Research RN (Day Shifts)Salt Lake City, UtahRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
Clinical Research RN (Night Shifts) CenExelClinical Research RN (Night Shifts)Salt Lake City, UtahProvides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.