Email Alert for
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.
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: MedixNorthwestern 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 UniversityAscension
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: AscensionShirley 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: MedasourceActalent
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: ActalentChicago, 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 partnership with the Principal Investigator (PI), Co-investigator(s), other study personnel, and sponsoring agents to ensure protocols are conducted in accordance with the principles of Good Clinical Practice (GCP) S/he will coordinate standard clinical research studies conducted by PI(s) which may include grant-funded, industry sponsored, and investigator-initiated clinical research studies. S/he will perform a variety of routine duties involving the collection, compilation, and documentation of clinical research data. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
Responsibilities:
•Recruits, consents, screens, schedules, tracks and provides study updates to study participants throughout the conduct of the study.
•Collects and enters data into study case report forms and/or electronic data capture system and respond to queries in a timely manner.
•May submit or coordinate the submission of study related documents, study protocols and study protocol amendments to the IRB per policy and procedure
•Maintains accurate and complete procedural documentation including study participant and site level documentation in compliance with institutional, local, state and federal guidelines and regulations related to clinical research.
•May collect, process and ship potentially biohazardous specimens.
•Administers structured tests and questionnaires according to research study protocols. May utilize study-related technology and equipment as part of assessment procedures.
•Provide ongoing study status updates and responds to questions from PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the conduct of the study
•Organize and participate in auditing and monitoring visits
•Gather and communicate unanticipated problems (protocol deviations, adverse events, and serious adverse events).
•Work with PI(s), sponsor, compliance, clinical staff and/or manager to identify and improve routine processes as it relates to the conduct of the research study
Required Job Qualifications:
•Bachelor's degree and 1 year of clinical research experience OR 5 years of clinical research experience.
•Demonstrated knowledge of Good Clinical Practices and Good Documentation Practices.
•Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research.
•Ability to meet deadlines and help coordinate multiple aspects of the ongoing project.
•Strong organizational and problem-solving skills.
•Detail oriented with high attention to accuracy.
•Ability to build rapport, navigates sensitive topics, and maintains confidentiality with a diverse pool of research participants and vendors.
•Effective verbal and written communication skills.
•Ability to collaborate within multi-disciplinary team settings.
•Availability to work evenings, overnight and weekends if called for under the study protocols.
•Travel may be required.
Preferred Job Qualifications:
•Bachelor's degree in Sciences or health-related discipline.
•Prior participant contact experience.
Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
Email Alert for Associate Clinical Research Coordinator jobs in Chicago, IL, United States
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.