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Merieux NutriSciences
Addison, IL, United States
Clinical Research Coordinator Addison Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related
Job Source: Merieux NutriSciencesMedix
Chicago, IL, United States
Manages daily operations of a biomedical &/or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors & other external project stakeholders. Monitors study performance, analyzes & review results, & supervises development & implementation of new protocols. May assign work & supervise study staff & reviews technical
Job Source: MedixAscension
Chicago, IL, United States
Details Department: Research Schedule: Full Time, Day Shifts Hospital: Ascension Saint Elizabeth Location: Chicago, Illinois Benefits Paid time off (PTO) Various health insurance options & wellness plans Retirement benefits including employer match plans Long-term & short-term disability Employee assistance programs (EAP) Parental leave
Job Source: AscensionActalent
Elmhurst, IL, United States
Description: Clinical Research Coordinator opening in Elmhurst, Il. The CRC will coordinate the execution of all clinical study protocol activities while maintaining Good Clinical Practice (GCP) and adhering to the Food and Drug Administration (FDA) regulations. The CRCs main responsibility is the conduct of multiple clinical trials, working closel
Job Source: ActalentInsight Global
Evanston, IL, United States
1. Communication and Coordination: o Check Emails and Voicemails: Start the day by reviewing emails and voicemails. Look for responses from potential funders, trial candidates, or medical professionals. o Coordinate with Key Personnel: Collaborate with the Principal Investigator (PI), department, and central administration to ensure that clinical
Job Source: Insight GlobalShirley Ryan AbilityLab
Chicago, IL, United States
By joining our team, you’ll be part of our life-changing Mission and Vision. You’ll work in a truly inclusive environment where diversity and equity are championed through words and actions. You’ll contribute to an innovative culture that is second to none, one that embraces curiosity, discovery and compassion. You’ll play a role in something that’
Job Source: Shirley Ryan AbilityLabCity of Hope
skokie, il
Registered Nurse - Clinical Research Coordinator Registered Nurse - Clinical Research Coordinator Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus,
Job Source: City of HopeRush
Chicago, IL, United States
Location: Chicago, IL Hospital: RUSH University Medical Center Department: Res-Recr - Mokhlesi Work Type: Full Time (Total FTE between 0.9 and 1.0) Shift: Shift 1 Work Schedule: 8 Hr (9:00:00 AM - 5:00:00 PM) Summary: This position works under the general direction of the Lung Center, their clinical department / division, and in partners
Job Source: RushEvanston, IL, United States
Clinical Research Coordinator
Location: Evanston, IL
Hours: Monday-Friday, standard business hours
Required Travel: Some local travel required
What you will need:
Education: Bachelor's degree preferred
Certification: CCRP (or similar) preferred.
Experience: At least two years of experience in coordinating clinical trials (experience with neurosciences/psychiatry/behavioral clinical trials highly preferred)
Skills: Phlebotomy skills highly preferred (phlebotomy skills will be required as part of the job); organizational and problem-solving abilities, effective communication, basic computer skills; highly compliant with respect to research policies and procedures
What you will do:
Coordinate and assist with multiple research studies (including in the areas of psychiatry, personalized medicine, outcome research, and family medicine)
Prepare sites for conducting the study, including assisting PIs with feasibility assessments
Develop Standard Operating Procedures, study forms, necessary database programs & data collection/entry strategies with applicable staff
Review & prepare correspondence with the Endeavor IRB (initial submission, protocol amendments, adverse events, yearly progress reports
Maintain regulatory documents as per sponsor & IRB protocols
Screen subjects for eligibility
Responsible for recruitment, coordination of care (in compliance with study protocol), and retention of research subjects
Participate in the Informed Consent process
Complete study activities as dictated by research protocols (including face to face and telephone assessments, medical records abstraction
Responsible for specimen collection, processing, and shipping
Coordinate & schedule appointments for diagnostic tests & procedures associated w/study protocols
Ensure that study documents are complete, current, and filed
Complete study close-out activities
Email Alert for Clinical Research Coordinator jobs in Evanston, IL, United States
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