1w
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Study Coordinator
Chicago, Illinois, United States
$22-$26/hr OnsiteFull Time
Supports non-clinical toxicology studies under GLP: protocol generation, study coordination, documentation; BS in natural sciences required; GLP familiarity and study support experience preferred.
Provantis
2w
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Clinical Study Coordinator
Zion, Illinois, United States
OnsiteFull Time
2+ YOECoordinate oncology clinical trials, ensure protocol and regulatory compliance, support participant recruitment and consent, maintain regulatory documentation. Requires bachelor's in science/health or equivalent experience, 2+ years clinical research, and specified certifications.
1d
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Study Director I
Itasca, Illinois, United States
$22-$35/hr OnsiteFull Time
Laboratory experience and study coordination in regulated environments, strong documentation and communication skills, scientific literacy, technical writing, and proficiency with Microsoft Office and laboratory systems; bachelor's in life sciences preferred.
Microsoft Office, laboratory information systems
1mo
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Clinical Study Coord
Duarte or Los Angeles or Orange County or Atlanta or Chicago or Phoenix
OnsiteFull Time
2+ YOEBachelor's in science/health preferred (substitutable by additional experience). Minimum 2 years research or clinical experience. Must obtain ACRP or SOCRA within 1 year; IATA, GCP, HSP, and BLS within 1 month. Understand/apply FDA, OHRP, GCP/ICH, HIPAA; execute protocols; coordinate recruitment/consent; monitor participants and report adverse even...
3w
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Power Systems Study Engineer III
United States or Colorado or California or Illinois or New York or Washington or District of Columbia
$105k-$131k/yr RemoteFull Time
5+ YOEBachelor's in electrical engineering (ABET), minimum 5 years electrical engineering experience, intermediate knowledge of power system studies (short-circuit, load flow, arc flash, protection coordination, transient stability), proficiency with ETAP/PSS/E/SKM/EasyPower and Microsoft Office, ability to work remotely and travel up to 10%.
SKM Powertools, EasyPower, ETAP, PSS/E, Microsoft Excel, Microsoft Word, Microsoft Outlook, Microsoft PowerPoint, Microsoft Teams
2w
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Study Abroad Program Manager
Elsah, Illinois, United States
$50k-$58k/yr OnsiteFull Time
2+ YOEBachelor's degree required, 2+ years program coordination or higher education experience, strong organizational and communication skills, proficiency with Microsoft Office, experience with international logistics preferred.
Microsoft Office Suite
3mo
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Research Coordinator-Pediatrics SPAH Kids Study (Spanish Speaking Preferred)
Evanston or Evanston
$25-$37/hr OnsiteFull Time
2+ YOEBS, 2 years research experience; Spanish speaking preferred; experience with recruitment, REDCap, SPSS; strong organization and communication.
REDCap, SPSS, Ripple
2mo
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Clinical Research Coordinator I
Chicago or United States
$50k-$65k/yr OnsiteFull Time
1+ YOEEntry-level clinical research coordinator supporting dental and health studies; coordinates visits, consents, data, and participant communications.
1mo
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Clinical Research Coordinator
McAllen or Texas or Louisiana or Illinois or Maryland or Kansas
OnsiteFull Time
2+ YOEBachelor's in a health-related field, 2+ years coordinating clinical research, knowledge of trial processes and regulatory requirements, familiarity with informed consent and study documentation, strong organizational skills.
Electronic data capture (EDC), Clinical trial management system (CTMS), Good Clinical Practice (GCP)
3w
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Clinical Research Coordinator II - Cardiology
Chicago, Illinois, United States
$50k-$82k/yr OnsiteFull Time
1+ YOEBachelor's degree with 1 year research experience required. Coordinates clinical study initiation, regulatory compliance (IRB, FDA, GCP, HSR), manages study documents and visits, collects specimens, and liaises with participants.
4w
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Clinical Research Coordinator
Springfield, Illinois, United States
$64k-$96k/yr OnsiteFull Time
Coordinate IRB-approved clinical trials, screen/consent/enroll patients, conduct study visits, manage investigational product, maintain source documentation and data entry, follow ICH/GCP/CFR/HIPAA, CPR required, Bachelor's degree required.
Microsoft Office, Electronic Medical Record (EMR)
1w
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Clinical Research Coordinator 2/3
Willowbrook, Illinois, United States
$67k/yr OnsiteFull Time
Coordinate clinical and observational trials in compliance with FDA/CFR and GCP; recruit and screen participants; perform assessments, regulatory documentation, data entry, and study drug accountability.
4w
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Project Coordinator Lead
Troy or California or Massachusetts or New York or Colorado or Hawaii or Illinois or Maryland or Minnesota or New Jersey or Vermont or Washington or District of Columbia
$78k-$155k/yr OnsiteFull Time
5+ YOEBachelor's degree or equivalent experience with 5+ years (or 4+ with related Master's); familiarity with Lean Six Sigma, analytical tools, workflow studies, project management, databases and data analytics; strong communication and organizational skills.
Lean Six Sigma, SAP, Solumina, JIRA, Tableau Dashboards
2w
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Clinical Research Coordinator
Chicago, Illinois, United States
$26-$43/hr OnsiteFull Time
2+ YOEBachelor's degree or equivalent, BLS certificate, ~2+ years clinical research experience, knowledge of GCP/ICH, ability to perform protocol procedures and maintain study documentation.
EDC
1w
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Financial Aid Coordinator
Chicago, Illinois, United States
$27/hr HybridFull Time
3+ YOE3 years combined education/office experience with 1 year of higher education/student services experience; experience with student employment, federal work study reconciliation, and supervising staff; background check required.
2mo
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Clinical Research Coordinator III - Emergency Medicine Clinical Trials
Chicago, Illinois, United States
$29-$43/hr OnsiteFull Time
3+ YOEBachelor's degree or equivalent experience, 3+ years coordinating clinical trials, independent site management, regulatory knowledge (GCP/NIH/FDA/IRB), ability to manage multiple studies, travel readiness, and mentorship ability.
2mo
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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
1d
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Account Coordinator I Employee Benefits
Kansas City or St Louis or Chicago or Saint Joseph
$24-$27/hr HybridFull Time
1+ YOEHigh school diploma/GED, 1-2 years insurance experience, strong verbal/written communication, proficiency with technology, ability to work independently and in teams, and maintain required licenses; expected to study for Life and Health Insurance exam.
Microsoft Office
2mo
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Substance Use Disorder ( SUD) Coordinator
Chicago, Illinois, United States
OnsiteFull Time
2+ YOEBachelor’s degree in addiction studies or social work; CADC or equivalent; 2 years SUD experience; knowledge of ASAM criteria; mission-aligned.
3w
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Clinical Trials Coordinator (Temp-to-Hire) - Chicago, IL
Chicago, Illinois, United States
$24-$32/hr OnsiteFull Time
2+ YOEMinimum 2 years CRC experience, strong phlebotomy skills, bachelor\u0002s degree required (advanced degree preferred), experience with metabolic/endocrine/internal medicine studies preferred, CCRC welcomed.
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