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Clinical data manager Jobs in Chicago, IL
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Clinical Research Data Manager
University of ChicagoChicago, IL, United States- Promoted
Manager, Data Analytics
HarnhamChicago, IL, United States- Promoted
Manager, Data Science
Press GaneyChicago, IL, United StatesClinical Case Manager
Heartland Human Care ServicesChicago, Illinois, United States, 60616- Promoted
Senior Clinical Research Data Manager
The University of ChicagoChicago, IL, United States- Promoted
Inpatient Clinical Manager
La Rabida Children's HospitalChicago, IL, USClinical Manager
IHMSChicago, Illinois, United StatesCLINICAL DATA ANALYST
Sinai Health System1500 S. California Avenue, Chicago, IL- Promoted
Market Data Manager
Selby Jenningschicago, IL, United States- Promoted
- New!
Manager - Data Analytics
DLA PiperChicago, IL, United States- Promoted
Manager, Data Governance
KPMGChicago, IL, United States- Promoted
Senior Manager, Clinical Data and Reporting Standards (Remote)
AbbVieChicago, IL, United States- Promoted
Clinical Account Manager
Alteas HealthChicago, IL, US- Promoted
- New!
Data Architect- Manager
PwCChicago, IL, United States- Promoted
Data Governance Manager
MavenSolve Consulting ServicesChicago, IL, United StatesPrincipal Clinical Data Managerv
Katalyst HealthCares & Life SciencesChicago, IL- Promoted
- New!
Data Analytics Manager
United AirlinesChicago, IL, United StatesClinical Case Manager
Keystone Advisors LLCChicago, IL, US- Promoted
Business Data Manager
Northern TrustChicago, IL, United States- Promoted
Clinical Manager RN
Rush University Medical CenterChicago, IL, United StatesClinical Research Data Manager
University of ChicagoChicago, IL, United States- Full-time
Location : Chicago, ILJob Description : Works on trials directly assigned. Works on industry sponsored trials which provide consistent monitoring / oversight.Assist senior staff maintain high enrolling studies.Accountable for all data management tasks in support of low complexity clinical research studies.Assist with document collection and review in collaboration with Principle Investigator (PI) while maintaining a high degree of confidentiality.Analyzes and organizes study-related documentation, such as protocol worksheets, adverse event reports, institutional review board documents, or progress reports.Assists with various professional, organizational, and operational tasks under direct supervision.Supports quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and / or samples.Performs other related work as needed.Preferred QualificationsEducation : Bachelors degree.Experience : Minimal medical / science related education or position.Preferred CompetenciesAbsorb large amounts of information quickly.Adaptability to changing working situations and work assignments.Attention to detail.Interact and communicate (verbal and written) with clarity, tact, and courtesy with patrons, sponsors, staff, faculty, students, and others.Organizational skills.Read and understand complex documents.Time management.Ability to work independently and as part of a team.Application DocumentsResume / CV (required)Cover Letter (required)#J-18808-Ljbffr