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Ascension
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: AscensionNorthwestern University
Chicago, IL, United States
Department: MED-Physical Med & Rehab Salary/Grade: EXS/5 Target hiring range for this position will be between $50,000-$65,000 per year. Offered salary will be determined by the applicant's education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data. Job Summary: Manages daily operations of
Job Source: Northwestern UniversityMerieux 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 NutriSciencesActalent
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 CRC's main responsibility is the conduct of multiple clinical trials, working close
Job Source: ActalentShirley 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 AbilityLabMedix
Hinsdale, IL, United States
Position Overview: In this role you will ensure IRB approved protocols are implemented and followed; execute the informed consent process and monitor patient status and safety; collect and organize research data; schedule and conduct study-specific training and site in-services to study related staff on new or amended protocols, and educate patient
Job Source: MedixMedasource
Evanston, 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 neuroscien
Job Source: MedasourceInsight 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 GlobalChicago, 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 operations ensuring that all processes, protocols & procedures are quality controlled & functioning up to standards. May co-author scientific papers for presentation & publication & coordinates writing, submission & administration of grants. Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) & all current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH).
This position is responsible for overseeing, organizing and implementing multiple clinical research trials being conducted .This individual ensures appropriateness of patients supervises data collection and reporting, patient management and ensures adherence to all regulatory requirements and sponsor protocols. In addition, this individual will act as a resource to research study patients, physicians and other clinic personnel.
Specific Responsibilities:
Leads execution & control of a biomedical &/or social science project or research study.
Manages and ensures completion of study activities per protocol. Collaborating with nursing staff and Principal Investigator (PI) ascertains pretreatment & eligibility requirements; interviews participants & obtains social & medical histories; based on results determines & registers participants with appropriate sponsors; completes informed consent; determines & organizes patient's treatment and test schedules.
Manages conduct of experimental tests & procedures. Closely monitors & documents patient's adverse events; partners with nursing staff in modifying dosages, tests & treatment schedule.
Reviews medical, laboratory, and other diagnostic data on study subject. Notifies principal investigator of any abnormal values or any significant changes in these values. Notifies and follows up with subjects as required.
Reviews any adverse events with assigned resource nurse and reports serious adverse events to principal investigator and sponsor in a timely manner. Follow up with subjects or subject family members in accordance with procedures. Prepares for and completes close out procedures for terminated studies.
May Perform blood draws, EKGs and other study specific procedures as required.
Email Alert for Clinical Research Coordinator jobs in Chicago, IL, United States
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