Rush University Medical Center
Associate Clinical Research Coordinator-19525
Rush University Medical Center, Chicago, Illinois, United States, 60290
Associate Clinical Research Coordinator-19525
Join to apply for the
Associate Clinical Research Coordinator-19525
role at
Rush University Medical Center Associate Clinical Research Coordinator-19525
Join to apply for the
Associate Clinical Research Coordinator-19525
role at
Rush University Medical Center Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Anesthesia Support
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (8:00:00 AM - 4:30:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $23.12 - $32.66 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
Summary
This position works under the general direction of the Office of Research Affairs' Clinical Research Administration Division, 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.
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.
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
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. Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Hospitals and Health Care Referrals increase your chances of interviewing at Rush University Medical Center by 2x Get notified about new Clinical Research Coordinator jobs in
Chicago, IL . Chicago, IL $46,280.00-$75,670.40 4 days ago Chicago, IL $64,015.00-$74,523.00 2 months ago Chicago, IL $50,000.00-$65,000.00 3 days ago Streeterville, IL $46,280.00-$75,670.40 1 month ago Streeterville, IL $46,280.00-$75,670.40 1 month ago Chicago, IL $50,000.00-$65,000.00 1 month ago Evanston, IL $68,000.00-$75,000.00 3 days ago Clinical Research Coordinator - Ophthalmology Clinic
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Join to apply for the
Associate Clinical Research Coordinator-19525
role at
Rush University Medical Center Associate Clinical Research Coordinator-19525
Join to apply for the
Associate Clinical Research Coordinator-19525
role at
Rush University Medical Center Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Anesthesia Support
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (8:00:00 AM - 4:30:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $23.12 - $32.66 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
Summary
This position works under the general direction of the Office of Research Affairs' Clinical Research Administration Division, 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.
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.
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
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. Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Hospitals and Health Care Referrals increase your chances of interviewing at Rush University Medical Center by 2x Get notified about new Clinical Research Coordinator jobs in
Chicago, IL . Chicago, IL $46,280.00-$75,670.40 4 days ago Chicago, IL $64,015.00-$74,523.00 2 months ago Chicago, IL $50,000.00-$65,000.00 3 days ago Streeterville, IL $46,280.00-$75,670.40 1 month ago Streeterville, IL $46,280.00-$75,670.40 1 month ago Chicago, IL $50,000.00-$65,000.00 1 month ago Evanston, IL $68,000.00-$75,000.00 3 days ago Clinical Research Coordinator - Ophthalmology Clinic
Chicago, IL $50,000.00-$65,000.00 1 month ago Oak Brook, IL $75,000.00-$85,000.00 2 days ago Chicago, IL $49,920.00-$81,619.20 2 weeks ago Chicago, IL $49,920.00-$81,619.20 2 months ago Chicago, IL $60,000.00-$75,000.00 1 month ago Streeterville, IL $49,920.00-$81,619.20 1 month ago Chicago, IL $60,000.00-$75,000.00 2 weeks ago Chicago, IL $51,346.00-$55,000.00 4 days ago Chicago, IL $49,920.00-$81,619.20 1 month ago Streeterville, IL $49,920.00-$81,619.20 1 month ago Clinical Research Coordinator I- Neonatology
Streeterville, IL $46,280.00-$75,670.40 1 month ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr