22 edc jobs at 14 companies in Orland Park, 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
3w
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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
3w
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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
2w
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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
4w
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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
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
3w
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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
1w
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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
6h
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Clinical Trial Manager
San Francisco or South San Francisco or Chicago or Belgium
$150k-$165k/yr OnsiteFull Time
5+ YOEBachelor's degree in life sciences or related field; 5–7 years in biotechnology or pharmaceutical clinical operations; global trial, CRO, vendor, regulatory, and Phase I–III experience; Excel and clinical systems proficiency.
Microsoft Excel, EDC, IRT, TMF, CTMS
2w
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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
3mo
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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
3w
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Senior Data Team Lead (Remote)
Anaheim or Atlanta or Austin or Boston or Charleston or Charleston or Charlotte or Chicago or Dallas or Durham or Jacksonville or Jersey City or Las Vegas or Miami or Myrtle Beach or New York or Norfolk or Oakland or Orlando or Philadelphia or Portland or Portland or Raleigh or Richmond or San Diego or San Francisco or Tampa or Virginia Beach
$87k-$217k/yr RemoteFull Time
7+ YOE5+ MgmtBachelor’s in life/health/clinical/biological/mathematical field,7+ years clinical data management experience,5+ years lead experience,experience with large global studies,knowledge of GCP/ICH,excellent communication and leadership.
Medidata Rave, Oracle InForm, EDC
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
3w
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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
3w
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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
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