NewExperienced 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 II - Oncology, Ophthalmology & Neurology - Central US Thermo Fisher Scientific IncClinical Research Associate II - Oncology, Ophthalmology & Neurology - Central USChicago, IL$66,800–$125,000 / yearWhat You'll Do: Monitors 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.
NewExperienced Clinical Research Associate (Level II) - FSP - Alzheimer's - Central US Thermo Fisher ScientificExperienced Clinical Research Associate (Level II) - FSP - Alzheimer's - Central USChicago, IllinoisWhat You’ll Do: • Monitors 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.
Research Coordinator-Cardiology Endeavor HealthResearch Coordinator-CardiologyGlenview, IL$24.86–$37.29 / hourOur more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals - Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) - all recognized as Magnet hospitals for nursing excellence. Endeavor Health is a fully integrated healthcare delivery system committed to providing access to quality, vibrant, community-connected care, serving an area of more than 4.2 million residents across six northeast Illinois counties.
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.
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 Coordinator 3 University of ChicagoClinical Research Coordinator 3Chicago, IL$65,000–$80,000 / yearAreas of expertise include anxiety and mood disorders, autism spectrum disorders, bipolar disorder and schizophrenia, dementia and cognitive disorders, eating disorders, obesity and related behavioral health conditions, substance use disorders, and impulse control and related disorders. The Clinical Research Coordinator III serves as a key point of contact for participating sites, study personnel, and research participants and their families, helping ensure study activities are completed accurately, consistently, and according to established timelines and requirements.
Clinical Research Associate - Start up - Cross TA IREClinical Research Associate - Start up - Cross TAChicago, Illinois$91,336–$114,170 / yearClinical Research Associate (Start up) - Cross Therapeutic Area- Illinois ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Collaborate with country operations teams to identify, select, and activate clinical trial sites in accordance with project timelines and requirements.
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.
Clinical Research Coordinator Associate FSM/CC Northwestern UniversityClinical Research Coordinator Associate FSM/CCChicago, IL$51,350–$73,890 / yearThe available benefits package for this position will include health, dental, vision, disability, and life insurance; paid vacation and holidays; paid medical/sick and parental leave; tuition benefits for the employee and dependents; pre-tax and flex spending accounts for commuting and dependent care; generous retirement savings options; and wellness programs. Job Summary: Coordinates non-therapeutic (i.e., minimal risk, survey, chart review) clinical research protocols with direction from the Principal Investigator and/or senior staff in compliance with regulatory laws and institutional guidelines.
Associate Clinical Research Coordinator Northwestern UniversityAssociate Clinical Research CoordinatorChicago, IL$51,350–$60,000 / yearThe available benefits package for this position will include health, dental, vision, disability, and life insurance; paid vacation and holidays; paid medical/sick and parental leave; tuition benefits for the employee and dependents; pre-tax and flex spending accounts for commuting and dependent care; generous retirement savings options; and wellness programs. Job Summary: Coordinates non-therapeutic (i.e., minimal risk, survey, chart review) clinical research protocols with direction from the Principal Investigator and/or senior staff in compliance with regulatory laws and institutional guidelines.
Clinical Research Coordinator Merieux NutriSciences CorpClinical Research CoordinatorAddison, ILThis position acts as a point person for the clinical-study site, overseeing all operational responsibilities for the successful launch, enrollment, maintenance and completion of clinical projects. Purpose (Objective): The Clinical Research Coordinator is an essential team member in the conduct of dietary, exercise and pharmaceutical studies.
NewResearch Assistant - Neuroimaging and Behavioral Data Rosalind Franklin University of Medicine and ScienceResearch Assistant - Neuroimaging and Behavioral DataNorth Chicago, IL$16–$20 / hourThe Research Assistant will help convert existing datasets and documentation into organized, quality-reviewed, analysis-ready resources; execute approved analyses; and prepare clear outputs for PI review and research dissemination. The Human Performance Laboratory and CLEAR at RFUMS is seeking a part-time Research Assistant to support Dr. Shawn Flanagan with the analysis, review, quality control, and organization of neuroimaging and behavioral data collected in recent studies.
Post-Doctoral Fellow, Research - Drs. Richard Lieber and Ishan Roy Shirley Ryan AbilityLabPost-Doctoral Fellow, Research - Drs. Richard Lieber and Ishan RoyChicago, Illinois$47,300–$78,700 / yearThe 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.
Competitive Research Analyst StratAcuity Staffing Partners IncCompetitive Research AnalystChicago, IL$40–$50 / hourIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Everforth Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts.
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.
FSP 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.
Clinical Research Project Manager Northwestern UniversityClinical Research Project ManagerChicago, IL$63,079–$78,849 / yearOversees day-to-day operations including identifying & securing needed resources; creating, implementing, monitoring, & updating project plans; facilitating meetings with appropriate parties; tracking tasks/deliverables to ensure timelines, milestones &/or goals are attained; monitoring & reporting progress as appropriate; & resolving or escalating issues in a timely manner. Collaborating with nursing staff and Principal Investigator (PI) ascertains pretreatment & eligibility requirements; interviews participants & obtains social & medical histories; based on results determines & registers participants with appropriate sponsors; completes informed consent; determines & organizes patients treatment and test schedules.
Clinical Research Coordinator, Gastroenterology Northwestern UniversityClinical Research Coordinator, GastroenterologyChicago, IL$51,350–$66,380 / yearCollaborating with nursing staff and Principal Investigator (PI) ascertains pretreatment & eligibility requirements; interviews participants & obtains social & medical histories; based on results determines & registers participants with appropriate sponsors; completes informed consent; determines & organizes patient's treatment and test schedules. Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) & all current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH).
Clinical Research Project Manager, Hematology Oncology Northwestern UniversityClinical Research Project Manager, Hematology OncologyChicago, IL$63,079–$88,705 / yearOversees day-to-day operations including identifying & securing needed resources; creating, implementing, monitoring, & updating project plans; facilitating meetings with appropriate parties; tracking tasks/deliverables to ensure timelines, milestones &/or goals are attained; monitoring & reporting progress as appropriate; & resolving or escalating issues in a timely manner. Collaborating with nursing staff and Principal Investigator (PI) ascertains pretreatment & eligibility requirements; interviews participants & obtains social & medical histories; based on results determines & registers participants with appropriate sponsors; completes informed consent; determines & organizes patients treatment and test schedules.