79 clinical study jobs at 37 companies in Illinois
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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...
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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
1w
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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
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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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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
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Research Study Coordinator
Chicago, Illinois, United States
$20-$25/hr OnsiteFull Time
2+ YOECoordinate clinical research activities, obtain consent, collect and analyze data, perform basic clinical procedures, complete IRB CITI training; bachelor's degree or equivalent and 2 years research experience required.
Microsoft Word, Microsoft Excel
3mo
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Clinical Trials Manager
Chicago, Illinois, United States
$60k-$85k/yr RemoteFull Time
2+ YOEManages and coordinates complex clinical trials; oversees protocol coordinators; ensures regulatory compliance and collaboration with study teams and external partners.
Regulatory Compliance, Clinical Trial Protocols, Project Coordination, Documentation, Stakeholder Communication
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Associate Director, Clinical Pharmacology/Senior Clinical Pharmacologist
North Chicago, Illinois, United States
$142k-$269k/yr HybridFull Time
0+ YOEAdvanced degree in clinical pharmacology or related field with substantial PK/PD, PBPK, pharmacometrics or drug metabolism experience; ability to lead teams, design Phase 1-4 studies, author regulatory documents, and engage with KOLs and regulators.
2w
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Sr. Director, Clinical Affairs
Lincolnshire, Illinois, United States
$210k-$330k/yr OnsiteFull Time
15+ YOE8+ MgmtMaster's required (medical/science preferred),15+ years clinical research experience,8+ years leading clinical projects,IVD study design expertise,GCP/GLP knowledge,lab instrument experience,ability to manage clinical strategy and regulatory submissions.
Microsoft Office, Microsoft Outlook, Adobe, LIS
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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
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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.
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Clinical Strategy Lead
Lexington or Atlanta or Chicago or Washington or New York City
$125k-$195k/yr RemoteFull Time
3+ YOEDegree in medicine, life sciences, allied health, pharmacy, or nursing; 3+ years industry experience in medical device/pharma; clinical research and study design experience; strong written/verbal English and Microsoft Office skills.
Microsoft Office
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.
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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)
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Clinical Trial Manager
Chicago or Minneapolis or Dallas or Houston or Austin or United States
$95k-$125k/yr RemoteFull Time
5+ YOEBachelor's in science/health required, minimum 5 years relevant experience, knowledge of ICH/FDA/European regulations, proficiency with Microsoft Word/Excel/PowerPoint, excellent communication, ability to manage clinical study sites and vendors; travel up to 25%.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1w
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Clinical Research Coordinator II - Radiation Oncology
Shiloh or Florissant
$55k-$82k/yr OnsiteFull Time
2+ YOEBachelors or equivalent, 2 years clinical research experience, BLS certification within 1 month of hire, experience with clinical study protocols and data management.
SAS
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)
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
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Experienced Clinical Research Associate - Sponsor Dedicated
North Carolina or Rhode Island or Maine or Ohio or Arizona or Delaware or Tennessee or Louisiana or Maryland or Michigan or Colorado or Connecticut or District of Columbia or Hawaii or North Dakota or New York or Virginia or Georgia or Wisconsin or New Hampshire or Arkansas or Vermont or Mississippi or Alaska or Washington or Montana or Missouri or Texas or Kansas or Illinois or Oklahoma or California or Nevada or Florida or West Virginia or Idaho or Pennsylvania or Indiana or Nebraska or Utah or New Mexico or New Jersey or South Dakota or Kentucky or South Carolina or Alabama or Wyoming or Massachusetts or Minnesota or Iowa or Oregon or Puerto Rico or Canada
RemoteFull Time
Bachelor's degree or RN (or equivalent), knowledge of ICH/GCP, strong computer and communication skills, ability to travel up to 75%, and audit/readiness experience for clinical studies.
1mo
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Clinical Dietician
Chicago, Illinois, United States
$35-$53/hr OnsitePart Time
3+ YOEBachelor's in Dietetics or Food and Nutrition Science, Illinois clinical dietician license, 3 years clinical experience and 3 years nutrition support experience; ability to develop nutrition care plans and perform metabolic cart studies.
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