2mo
Save
Mark Applied
Hide
IRB Reliance Analyst
Chicago or Evanston
$69k-$78k/yr OnsiteFull Time
2+ YOEBachelor's degree required, 2+ years related experience, knowledge of human subjects regulations, CIP/CIM eligibility within a year, strong communication, computer proficiency, report writing, and ability to work evenings/weekends as needed.
eIRB+, Huron’s Click® IRB software, HRPP Toolkit
2mo
Save
Mark Applied
Hide
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
5d
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
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.
3d
Save
Mark Applied
Hide
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
3d
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
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
3d
Save
Mark Applied
Hide
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
1w
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
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)
1mo
Save
Mark Applied
Hide
Research Coordinator, Advocate Aurora Research Institute
Kenosha, Wisconsin, United States
$31-$46/hr OnsiteFull Time
2+ YOECoordinates clinical research protocols including study start-up, IRB submissions, recruitment/enrollment, data collection (EDC), monitoring, and regulatory compliance. Requires bachelor's degree, ~2 years research experience, GCP/ICH/FDA knowledge, EMR and Microsoft Office proficiency.
CTMS, EDC, Electronic Medical Record (EMR), Microsoft Office Suite
Explore Jobs
Expand Your Job Search
Top Cities Near Elgin for Irb
- Irb jobs in Chicago, IL
- Irb jobs in Aurora, IL
- Irb jobs in Rockford, IL
- Irb jobs in Joliet, IL
- Irb jobs in Naperville, IL
- Irb jobs in Kenosha, WI
- Irb jobs in Waukegan, IL
- Irb jobs in Cicero, IL
- Irb jobs in Arlington Heights, IL
- Irb jobs in Evanston, IL
- Irb jobs in Schaumburg, IL
- Irb jobs in Bolingbrook, IL
- Irb jobs in Palatine, IL
- Irb jobs in Skokie, IL
- Irb jobs in Des Plaines, IL
- Irb jobs in Orland Park, IL
- Irb jobs in Tinley Park, IL
- Irb jobs in Oak Lawn, IL
- Irb jobs in Berwyn, IL
- Irb jobs in Mount Prospect, IL