68 clinical study jobs at 29 companies in Elgin, IL
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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
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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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
1mo
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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
1w
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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
1mo
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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 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
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
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.
2mo
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Senior Clinical Research Associate (level dependent on experience)
Chicago, Illinois, United States
RemoteFull Time
Experience in monitoring, site management, and study documentation; degrees in allied health or nursing; RN possible.
Clinical Monitoring Software, CRF/Source Document Review, Regulatory Documentation Systems
1w
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Program Implementation Manager, Clinical Studies
Dallas or New York or Chicago or Philadelphia
$70k-$90k/yr RemoteFull Time
3+ YOE3+ years experience managing clinical study site activation, recruitment, and site-level process improvement; strong project management, account management, and communication skills; Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
1w
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Research Coordinator - Surgery Research
Evanston, Illinois, United States
$25-$37/hr OnsiteFull Time
1+ YOECoordinate clinical research studies, perform phlebotomy and ECGs, maintain regulatory files, train junior staff, and manage study finances; bachelor's degree preferred; 1-3 years research experience; CITI training required.
2w
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Physician Assistant or Nurse Practitioner - Family Medicine - (Gauthier)
Pleasant Prairie, Wisconsin, United States
OnsiteFull Time
Master's or doctorate in PA/NP studies, state license in Wisconsin (PA or RN+APNP), national certification (NCCPA or ANCC), clinical documentation skills, and ability to provide primary care in a family medicine clinic.
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