19 edc jobs at 14 companies in Des Plaines, IL
1mo
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Specialist Clinical Data Management
Libertyville, Illinois, United States
$77k-$120k/yr OnsiteFull Time
2+ YOEBachelor's degree with minimum 2 years clinical data/EDC experience, EDC database programming and data monitoring skills, clinical research/regulatory knowledge, CCDM preferred, proficiency with Medrio/Clinpal/Medidata Rave and Microsoft Office.
EDC System, Medrio, Clinpal, Medidata Rave, Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Teams
2w
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System Design Analyst II - HYBRID
North Chicago, Illinois, United States
$85k-$162k/yr HybridFull Time
5+ YOEBachelor's degree,5+ years hands-on EDC study build experience with Medidata RAVE required; CDASH and SDTM knowledge; EMR integrations, coaching/mentoring and strong communication.
Medidata RAVE, Veeva EDC, EDC, CDASH, SDTM
2w
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(Senior) Clinical Study Manager, Clinical Development
Research Triangle Park or Chicago
$110k-$160k/yr OnsiteFull Time
5+ YOE5+ years clinical trial management experience in biotech/pharma/CRO, Bachelor's in life sciences or nursing required; EDC/CTMS/eTMF proficiency, familiarity with SQL, oncology or molecular diagnostics experience.
EDC, CTMS, eTMF, SQL
1w
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Clinical Research Coordinator II (4066)
Melrose Park, Illinois, United States
$60k-$78k/yr OnsiteFull Time
2+ YOE2+ years CRC experience preferred, HS diploma required (Bachelor's preferred), ICH-GCP and IATA training, ACRP preferred, EDC/IVRS proficiency, ability to consent patients and maintain trial documentation.
EDC, IVRS
1mo
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Systems Design Analyst II
North Chicago or Irvine
$110k-$209k/yr HybridFull Time
5+ YOEBachelor's (Masters preferred). 5+ years clinical technology experience (EDC, IRT, ePRO) or 7+ years similar role. In-depth clinical trial and CDASH/SDTM knowledge, strong communication, mentoring, and regulatory compliance experience.
EDC, IRT, ePRO, CDASH, SDTM
3w
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Senior Clinical Research Associate, Field Monitor
El Segundo or Los Angeles or San Diego or San Francisco or New York City or Chicago or Boston
$128k-$136k/yr RemoteFull Time
6+ YOEBachelor's degree (or RN with 5+ years monitoring),6+ years clinical trial experience,4+ years on-site/remote monitoring,valid driver's license,knowledge of ICH‑GCP,EDC/eTMF/CTMS and MS Office,ability to travel 50–75%.
EDC, eTMF, CTMS, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Adobe
1mo
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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
3mo
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Clinical Research Coordinator
Oak Brook, Illinois, United States
OnsiteFull Time
1+ YOE1-2 years clinical research experience preferred; MSK and cardiometabolic experience preferred; manage multiple studies; phlebotomy; CRIO CTMS, eSource, eRegulatory preferred; EDC data entry required; IRT familiarity preferred; regulatory documentation; GCP; strong organization and communication; CRC certification a plus.
CRIO CTMS, eSource, eRegulatory, EDC, IRT
1mo
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Lead Clinical Research Data Manager
Chicago, Illinois, United States
$65k-$80k/yr HybridFull Time
5+ YOECollege/university degree required; 5+ years related experience; advanced data management skills; supervisory experience possible; proficiency with Word, Excel, and EDC systems.
Microsoft Word, Microsoft Excel, Adobe Acrobat, RAVE, Inform, RedCap
2w
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Clinical Research Coordinator
Chicago, Illinois, United States
OnsiteFull Time
3+ YOE3+ years clinical research coordination experience preferred; bachelor's in life sciences/nursing/healthcare preferred; experience with study start-up, regulatory submissions, EDC and MS Office; strong communication and organizational skills.
Electronic Data Capture (EDC), Microsoft Office
2w
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Data Assistant Sr FSM/CC
Chicago, Illinois, United States
$51k-$74k/yr OnsiteFull Time
1+ YOECoordinate and maintain clinical research data, enter and validate case report forms, conduct chart audits, assist with audits/inspections, and serve as team lead; HS diploma required, 1+ years clinical research experience preferred.
eIRB, Kronos, Mac OS X, Microsoft Exchange, CTMS, EDC, Rave, Redcap
1w
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Registered Nurse - Acute Dialysis RN
Chicago or Oak Park
$39-$55/hr FieldFull Time
Current RN license, ADN, and dialysis experience required. Acute care experience is helpful but not required; candidates must pass a color vision test.
ICU, CCU, ED, CRRT, PCTs
1mo
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Senior Global Clinical Study Manager
Chicago or Dallas or Durham or Gilbert or Indianapolis or New York or Phoenix or Rockville or San Francisco or Tampa
$93k-$233k/yr RemoteFull Time
5+ YOE2+ MgmtBachelor's in life sciences,5+ years clinical research experience including 2+ years clinical study management; oncology and global trial experience; knowledge of ICH-GCP, regulatory requirements, financial management.
Microsoft Office, CTMS, EDC
2w
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Clinical Research Coordinator I (CRC-1)
Chicago, Illinois, United States
OnsiteFull Time
1+ YOESupport clinical trial coordination including recruitment, consent, data entry, and regulatory compliance; bachelor's preferred; 0–1 years clinical/research experience; clinical research certification expected within 18 months.
EHR, EDC, CTMS
1d
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Medical Technologist or Medical Lab Technician - Transfusion Services/Full-Time/2nd Shift/Lutheran General
Park Ridge, Illinois, United States
$24-$46/hr OnsiteFull Time
Associate degree or approved medical laboratory technician program required; no experience or license required. Requires communication skills, stress management, confidentiality, and ability to operate laboratory equipment.
CAP, ED, ICU, OR
1mo
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Senior Global Clinical Study Manager
Durham or Phoenix or Gilbert or San Francisco or New York City or Indianapolis or Tampa or Rockville or Chicago or Dallas
$93k-$233k/yr OnsiteFull Time
5+ YOE2+ MgmtBachelor's in life sciences, 5+ years clinical research/monitoring (including 2 years study management), Phase III and oncology experience, ICH-GCP and FDA knowledge, global trial and financial management, stakeholder leadership.
Microsoft Office, CTMS, EDC
2mo
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Clinical Research Coordinator III
Chicago, Illinois, United States
OnsiteFull Time
5+ YOEOversee site-based clinical research activities, ensure regulatory compliance, manage training, data entry, and sponsor communications; minimum 5 years in clinical research; bilingual Spanish a plus.
EDC, IVRS, SOPs
2mo
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Clinical Research Coordinator I
Chicago, Illinois, United States
OnsiteFull Time
1+ YOEEntry-level CRC role requiring high school diploma; experience in clinical research preferred; bilingual Spanish preferred.
EDC, IVRS, Laboratory Equipment
2w
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Clinical Research Sub-Investigator / Principal Investigator
Chicago, Illinois, United States
OnsiteFull Time
0+ YOELicensed MD/DO/NP/PA with ability to obtain Illinois license; PI track requires 5+ years research experience; GCP/ICH-GCP knowledge; ability to perform exams, consent, and safety monitoring; strong communication skills.
Microsoft Office, CTMS, EDC
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