3mo
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IRB Compliance Analyst
Chicago or Evanston
$69k-$78k/yr OnsiteFull Time
2+ YOEBachelor's degree, eligible for CIP exam, 2+ years related experience, knowledge of federal/state human research regulations, computer proficiency, report writing, strong communication and multi-tasking skills.
Huron’s Click® IRB software, HRPP Toolkit
1w
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MEDICAL EDUCATION AND IRB COORDINATOR
Kankakee, Illinois, United States
$26-$34/hr OnsiteFull Time
Bachelor's degree required; strong organizational, communication, and interpersonal skills; proficiency in Microsoft Word, Excel, PowerPoint, and Outlook; ability to maintain confidentiality and prioritize multiple projects; knowledge of research/regulatory compliance preferred.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
2mo
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Clinical Research Coordinator II
Chicago, Illinois, United States
$60k-$75k/yr OnsiteFull Time
2+ YOEExperience coordinating clinical trials, patient recruitment, data management; 2-5 years; Bachelor's degree preferred; knowledge of IRB, SOPs, regulatory compliance.
IRB, SOP, CRF, Clinical trial management, Laboratory procedures
3d
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Research Compliance Specialist II
Chicago, Illinois, United States
$72k-$88k/yr RemoteFull Time
2+ YOEBachelor's degree or equivalent, minimum 2 years IRB/COI experience, U.S. work authorization, proficiency in Microsoft Word and Excel and Adobe Acrobat, experience with electronic IRB/COI systems, knowledge of federal research and COI regulations.
Microsoft Word, Adobe Acrobat, Microsoft Excel, Huron HRPP Toolkit, HRS IRB
2mo
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Clinical Research Coordinator I-Emergency Medicine (Evening Shift)
Chicago, Illinois, United States
$46k-$76k/yr OnsiteFull Time
Bachelor’s degree required; supports regulatory docs, IRB processes, subject recruitment, data handling; strong organizational, communication, and FDA/HSR/GCP knowledge.
2w
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Clinical Research Specialist SMS-3817
Springfield, Illinois, United States
$3k-$4k/mo OnsiteFull Time
Bachelor's degree required; supports clinical research activities, gathers and maintains study documentation, assists with IRB submissions and data collection, and communicates with staff and monitors.
Microsoft Access, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Electronic Medical Records (EMR)
1d
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Visiting Research Specialist -DOM: Center for Dissemination and Implementation Science
Chicago, Illinois, United States
$65k-$75k/yr OnsiteFull Time
3+ YOEBachelor's in social science required (Master's preferred). Minimum 3 years research experience, knowledge of research protocols, team management, IRB/regulatory compliance, grant and manuscript support.
REDCap
1mo
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Coordinator Simulation Research
Peoria, Illinois, United States
$29-$34/hr OnsiteFull Time
1+ YOEBachelor's in sciences (or equivalent research experience), 1 year research experience, knowledge of IRB/FDA/compliance, MS Office proficiency, analytical and interpersonal skills, professional typing ability.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Qualtrics, Select Survey, Nvivo, MaxQDA, Microsoft Access, Blackboard, Canvas
1d
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Mgr, Quality Evaluation
Itasca, Illinois, United States
$102k-$108k/yr OnsiteFull Time
2+ YOEBachelor's required, 2+ years evaluation or public health experience, quantitative/qualitative analysis, database management, dashboarding, IRB/MOC/CME familiarity, strong communication and project management.
SPSS, Atlas.ti, PowerBI, REDCap, SharePoint, Zoom, Teams, WebEx
1mo
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Project Coordinator - Emergency Medicine
New York City or Chicago or New Haven
$70k-$77k/yr OnsiteFull Time
3+ YOEBachelor's degree plus 3 years related experience; experience managing multi-site clinical research, NIH/IRB compliance, regulatory reporting, site coordination, and data quality monitoring.
REDCap, Modus, ClinicalTrials.gov, SharePoint, NIHMS, PubMed Central, RPPRs, SMS
1mo
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Regulatory Compliance Coordinator
Springfield, Illinois, United States
$69k-$104k/yr OnsiteFull Time
3+ YOEBachelor's in chemical/biological sciences or equivalent; 3+ years clinical research or regulatory experience; strong knowledge of GCP/ICH/CFR/HIPAA; familiarity with IRB submissions and auditing; preferred CCRP or CCRC.
Microsoft Windows, Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Adobe Reader, Adobe DC
1d
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Visiting Research Specialist-DOM: Center for Dissemination and Implementation Science
Chicago, Illinois, United States
$65k-$75k/yr OnsiteFull Time
3+ YOEBachelor's in social science (Master's preferred), 3+ years research experience coordinating community-based health studies, IRB and regulatory experience, supervisory and project management skills, bilingual English/Spanish.
REDCap, Microsoft Office
1d
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Research Regulatory Coordinator
Urbana, Illinois, United States
$26-$43/hr HybridFull Time
Experience with clinical research regulatory processes, IRB/HIPAA compliance, informed consent review, CITI training, and CCRP certification within 3 years; bachelor's degree or equivalent experience in a related field.
CITI
3d
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Research Scientist
Seattle or Arizona or California or Colorado or Connecticut or Florida or Georgia or Illinois or Massachusetts or New Jersey or New Mexico or New York or Ohio or Oregon or Pennsylvania or Texas or Virginia or Washington
$84k-$100k/yr RemoteFull Time
Committee for Children: Research-based social-emotional learning and child safety programs.
3+ YOEMaster's required; 3+ years conducting K-12 program evaluation or product research; IRB experience; survey, interview, and focus group design; descriptive and inferential analysis; strong communication and project management.
Microsoft Excel, Microsoft Forms, SPSS, R, NVivo
1w
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Clinical Research Coordinator III - Psychiatry
Chicago, Illinois, United States
$29-$43/hr OnsiteFull Time
3+ YOEBachelor's degree (or 4 years' coordinating experience), 3+ years coordinating clinical trials, GCP/regulatory knowledge, NIH/FDA/IRB compliance, project management, problem solving, audit readiness, travel as needed.
1mo
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Vice President of Clinical Research
Boston or New York or Chicago
$205k-$260k/yr HybridFull Time
10+ YOE10+ years in clinical trials operations with site-level or multi-site management, strong knowledge of GCP/ICH/FDA/IRB, sponsor/CRO negotiation and P&L ownership, proven team building and operational systems experience.
CTMS, eTMF
1mo
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UHI Research Coordinator
Chicago, Illinois, United States
$73k-$86k/yr OnsiteFull Time
2+ YOEBachelor's required (Master's preferred); minimum 2 years experience in clinical research coordination, quality improvement, or community-based research; familiarity with QI and regulatory/IRB processes; proficiency with data management and EHR; strong organizational and communication skills; ability to travel locally.
Electronic Health Records (EHR)
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