Temporary Clinical Research Nurse Coordinator University of ChicagoTemporary Clinical Research Nurse CoordinatorChicago, IL$31.25–$38 / hourUnder the direction of the PI, Co-Investigators, Advanced Practice Registered Nurses (APRNs) and Research Manager (RM), the Clinical Research Nurse Coordinator oversees, facilitates, and participates in the conduct of daily activities of complex clinical trials and plays a critical role in the conduct of the studies to ensure compliance with federal and institutional regulations. The Institute for Population and Precision Health (IPPH), located in the Biological Sciences Division, integrates a wide spectrum of factors such as human health behaviors, environmental factors, social and economic factors, policies and genetic determinants of health, into studies focused on the treatment and prevention of disease, as well as the maintenance of wellness.
Clinical Research Coverage Analyst University of ChicagoClinical Research Coverage AnalystChicago, IL$65,000–$90,000 / yearAs a member of the Research Systems & Coverage Analysis (RSCA) Unit, within the Office of Clinical Research, the Coverage Analysts works as part of a team to support and optimize clinical trial initiation and financial workflows, partnering closely with research teams and key stakeholders in the process. The Office of Clinical Research (OCR) is dedicated to supporting the infrastructure for the management and administration of clinical research at The University of Chicago as well as individual research programs with the goal of improving communication, consistency, and collaboration across the Biological Sciences Division and UChicago Medicine.
Research Assistant Allen SpoldenResearch AssistantChicago, IllinoisThis is an excellent opportunity for recent graduates in Biology, Chemistry, Biochemistry, Biotechnology, Biomedical Science, or related life science disciplines who are looking to begin their careers in scientific research. As a Research Assistant, you will support laboratory experiments, collect and analyze research data, prepare laboratory materials, and assist scientists with ongoing research projects.
Clinical Research Associate II IREClinical Research Associate IIChicago, IllinoisWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Chicago 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.
Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available Thermo Fisher ScientificExperienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas AvailableChicago, IllinoisMonitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Clinical Research Associate - Cross TA IREClinical Research Associate - Cross TAChicago, IllinoisWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Illinois 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.
Senior Clinical Research Associate IRESenior Clinical Research AssociateChicago, IllinoisPerform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
Clinical Research Associate 2 IREClinical Research Associate 2Chicago, IllinoisICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Clinical Research Sub-Investigator / Principal Investigator Cedar Crosse Research CenterClinical Research Sub-Investigator / Principal InvestigatorChicago, IllinoisThis is one posting covering two possible entry points — where you land depends on your experience: Principal Investigator – for candidates with 5+ years of clinical research experience as a PI or Sub-Investigator, an active/unrestricted Illinois medical license (MD or DO), and the qualifications to hold ultimate regulatory and medical responsibility for assigned studies. For over 30 years and 550+ clinical trials, we've been a leading Midwest site conducting research across diabetes, hypertension, obesity, migraine, high cholesterol, heart disease, vaccines, kidney disease, pain, and more.
Clinical Research Financial Analyst University of ChicagoClinical Research Financial AnalystChicago, IL$70,000–$95,000 / yearActivities include but are not limited to supporting research revenue cycle management through research billing review, processing payments, reviewing and preparing research billing documentation, and producing research financial reporting, as well as department projects and initiatives to support research billing compliance tasks as needed. The OCR focuses on six key areas of service including: Human Subject Protection (IRB); Training and Education; Regulatory and Contract Oversight; Quality Assurance/Reporting and Auditing; Financial/Billing Compliance; Institutional Infrastructure.
NewResearch Site Clinical Staff Research by Design, LLCResearch Site Clinical StaffChicago, ILJob Description Responsible for assisting in the performance of clinical trials, including medication administration, dispensing, laboratory procedures, documentation whether in writing or electronic capture and completion of study visits, in accordance with the protocol and with protocol requirements. Performs IV set up, subcutaneous administration and PO medication and reconstitutes, dilutes and accurately measures protocol medications.
Clinical Research Coordinator II, Surgery University of ChicagoClinical Research Coordinator II, SurgeryChicago, IL$60,000–$75,000 / yearResponsibilities include, but are not limited to, provides efficient and complete data collection, processing, analysis and reporting; assures source documentation and data abstraction and entry are being done at the protocol specified time-points; ensures data accuracy and integrity by working closely with internal monitors and/or auditors to promptly resolve any data quality concerns or outstanding queries; and, facilitates the exchange of data across projects and organizations. Plans and coordinates subjects schedule for study procedures, return visits, and study treatment schedules; educates subjects about study procedures to be performed, what to report between and during visits, and the risks and benefits of the procedures; performs assessments at visits and monitors for adverse events.
Clinical Research Associate - Start up - Cross TA IREClinical Research Associate - Start up - Cross TAChicago, IllinoisCollaborate with country operations teams to identify, select, and activate clinical trial sites in accordance with project timelines and requirements. Coordinate with the country operations team to collect essential documents (such as regulatory approvals and contracts) to enable timely site activation.
NewResearch Assistant I Certified GroupResearch Assistant IAurora, ILCertified Group is comprised of a set of specialized brands that collectively deliver laboratory testing, regulatory consulting, and certification & audit services across highly regulated industries: Certified Laboratories – Provides comprehensive analytical and microbiological testing, primarily supporting food, beverage, cosmetics, OTC, and dietary supplement industries. *]:pointer-events-auto [content-visibility:auto] supports-[content-visibility:auto]:[contain-intrinsic-size:auto_100lvh] scroll-mt-[calc(var(--header-height)+min(200px,max(70px,20svh)))]"> The compensation details provided below reflect the expected pay range for this role, based on the selected compensation structure and applicable guidelines.
Clinical Research Project Manager University of ChicagoClinical Research Project ManagerChicago, IL$75,000–$90,000 / yearThe lab routinely collaborates across disciplines, departments, and with investigators at other institutions including experts in the fields of computer science, geriatrics, oncology, public health, social services administration, psychology, neuroscience, materials science, engineering and other medical and social science fields. Project management for high complexity clinical studies, including the scientific elements of study planning, monitoring, and execution of investigator-initiated research efforts and owning administrative tasks to ensure timely progress toward scientific milestones and deliverables.
NewFSP Clinical Research Associate 2 - Central Region Fortrea IncFSP Clinical Research Associate 2 - Central RegionILRemote$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.
NewClinical Research Nurse Coordinator Northwestern Memorial HealthCareClinical Research Nurse CoordinatorChicago, ILThe Clinical Research Nurse Coordinator is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (e.g., investigator initiated trials, sponsor trials) and Northwestern Memorial Hospital; a joint collaboration between Northwestern Memorial Hospital and the NU Feinberg School of Medicine. Collaborates with Clinical Coordinators, Education Coordinators, and peer CRNCs to identify training needed for clinical research nurses about unfamiliar practices, procedures and medications to ensure patient/subject safety and compliance with protocols and regulatory requirements.
Post-Doctoral Fellow, Research - Drs. Richard Lieber and Ishan Roy Shirley Ryan AbilityLabPost-Doctoral Fellow, Research - Drs. Richard Lieber and Ishan RoyChicago, IllinoisThe Post-Doctoral Fellow, Research will consistently demonstrate support of the Shirley Ryan AbilityLab statement of Vision, Mission and Core Values by striving for excellence, contributing to the team efforts and showing respect and compassion for patients and their families, fellow employees, and all others with whom there is contact at or in the interest of the institute. The fellow will lead interdisciplinary, translational research bridging muscle mechanics and multi-omics to uncover mechanisms of muscle dysfunction in chronic diseases (such as cancer) and inform precision rehabilitation strategies.
Research Scientist II Shirley Ryan AbilityLabResearch Scientist IIChicago, IllinoisThe Research Scientist II will consistently demonstrate support of the Shirley Ryan AbilityLab statement of Vision, Mission and Core Values by striving for excellence, contributing to the team efforts and showing respect and compassion for patients and their families, fellow employees, and all others with whom there is contact or in the interest of Shirley Ryan AbilityLab. You’ll play a role in something that’s never been done before as we integrate science and clinical care to help patients achieve better, faster outcomes — as we Advance Human Ability, together.
MRI Technical Specialist - Advanced and Research Imaging Ann & Robert H. Lurie Children's Hospital of ChicagoMRI Technical Specialist - Advanced and Research ImagingChicago, IllinoisEnsures enterprise-wide alignment between written MRI protocols, Epic orderables, and scanner-level builds while maintaining protocol documentation and version control to support operational consistency and reliability. Provides advanced technical oversight, real-time troubleshooting, and performance optimization across MRI scanners and clinical locations to ensure optimal performance and image quality.