Rush University
Senior Clinical Research Coordinator-20258
Join to apply for the
Senior Clinical Research Coordinator-20258
role at
Rush University Medical Center Senior Clinical Research Coordinator-20258
6 days ago Be among the first 25 applicants Join to apply for the
Senior Clinical Research Coordinator-20258
role at
Rush University Medical Center Get AI-powered advice on this job and more exclusive features. Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Cancer Center-Res Fac
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (8:00:00 AM - 5:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $29.36 - $42.61 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 Rushs 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 handles the more complex clinical research studies conducted by PI(s) which may include grant-funded, industry sponsored, and investigator-initiated clinical research studies. Partners with the PI to manage multiple complex clinical research studies. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
Required Job Qualifications
Bachelor's degree and 5 years of clinical research experience OR 9 years of clinical research experience. 5 years coordinating Human Subjects research. Demonstrated advanced knowledge of Good Clinical Practices and Good Documentation Practices. Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research. Relevant certification as a Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professionals (CIP). Strong project management skills. Demonstrated problem-solving, critical decision makings and professional judgement. Strong analytical and organizational skills with a high attention to details. Demonstrated ability to build rapport, navigate sensitive topics, and maintain confidentiality with a diverse pool of research participants and vendors. Strong verbal and written communication with ability to communicate complex concepts to multiple audiences. Demonstrated ability to collaborate within multi-disciplinary team settings. Travel may be required.
Preferred Job Qualifications
Bachelor's degree in science or health related field. Masters degree with science or health related field. Prior supervisory experience.
Responsibilities
Coordinates all aspects of complex studies, including recruitment, consent, screening, scheduling, and tracking and provides study updates to study participants throughout the conduct of the study. Ensures data is entered into the studys electronic data capture system and queries are responded to and resolved in a timely manner. Oversees the submission of study related documents, study protocols and study protocol amendments to the IRB per policy and procedure. Ensures procedural documentation is accurate, complete, and in compliance with institutional, local, state and federal guidelines and regulations related to clinical research. Oversees the collection, processing and shipment of potentially biohazardous specimens. Oversees the administration of structured tests and questionnaires according to research study protocols including the utilization of study-related technology and equipment as part of assessment procedures. Reviews and finalizes summary report(s) for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance and ensures accurate study updates are provided throughout the conduct of the study. Lead the development of any required action plans in conjunction with researcher. Ensure unanticipated problems (protocol deviations, adverse events, and serious adverse events) are submitted in a timely manner. Provide recommendations to proactively address complex issues and/or variances with study related activities. Train and mentor clinical research staff members within the department. May summarize and share relevant research during internal and external presentations. Maintains current knowledge of industry trends.
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
Mid-Senior level Employment type
Employment type
Full-time Job function
Job function
Research, Analyst, and Information Technology Industries
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Join to apply for the
Senior Clinical Research Coordinator-20258
role at
Rush University Medical Center Senior Clinical Research Coordinator-20258
6 days ago Be among the first 25 applicants Join to apply for the
Senior Clinical Research Coordinator-20258
role at
Rush University Medical Center Get AI-powered advice on this job and more exclusive features. Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Cancer Center-Res Fac
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (8:00:00 AM - 5:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $29.36 - $42.61 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 Rushs 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 handles the more complex clinical research studies conducted by PI(s) which may include grant-funded, industry sponsored, and investigator-initiated clinical research studies. Partners with the PI to manage multiple complex clinical research studies. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
Required Job Qualifications
Bachelor's degree and 5 years of clinical research experience OR 9 years of clinical research experience. 5 years coordinating Human Subjects research. Demonstrated advanced knowledge of Good Clinical Practices and Good Documentation Practices. Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research. Relevant certification as a Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professionals (CIP). Strong project management skills. Demonstrated problem-solving, critical decision makings and professional judgement. Strong analytical and organizational skills with a high attention to details. Demonstrated ability to build rapport, navigate sensitive topics, and maintain confidentiality with a diverse pool of research participants and vendors. Strong verbal and written communication with ability to communicate complex concepts to multiple audiences. Demonstrated ability to collaborate within multi-disciplinary team settings. Travel may be required.
Preferred Job Qualifications
Bachelor's degree in science or health related field. Masters degree with science or health related field. Prior supervisory experience.
Responsibilities
Coordinates all aspects of complex studies, including recruitment, consent, screening, scheduling, and tracking and provides study updates to study participants throughout the conduct of the study. Ensures data is entered into the studys electronic data capture system and queries are responded to and resolved in a timely manner. Oversees the submission of study related documents, study protocols and study protocol amendments to the IRB per policy and procedure. Ensures procedural documentation is accurate, complete, and in compliance with institutional, local, state and federal guidelines and regulations related to clinical research. Oversees the collection, processing and shipment of potentially biohazardous specimens. Oversees the administration of structured tests and questionnaires according to research study protocols including the utilization of study-related technology and equipment as part of assessment procedures. Reviews and finalizes summary report(s) for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance and ensures accurate study updates are provided throughout the conduct of the study. Lead the development of any required action plans in conjunction with researcher. Ensure unanticipated problems (protocol deviations, adverse events, and serious adverse events) are submitted in a timely manner. Provide recommendations to proactively address complex issues and/or variances with study related activities. Train and mentor clinical research staff members within the department. May summarize and share relevant research during internal and external presentations. Maintains current knowledge of industry trends.
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
Mid-Senior 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 Senior Clinical Research Coordinator jobs in
Chicago, IL . Chicago, IL $64,015.00-$74,523.00 1 month ago Streeterville, IL $46,280.00-$75,670.40 4 days ago Streeterville, IL $46,280.00-$75,670.40 1 month ago Evanston, IL $68,000.00-$75,000.00 2 weeks ago Streeterville, IL $46,280.00-$75,670.40 1 month ago Chicago, IL $50,000.00-$65,000.00 3 weeks ago Clinical Research Coordinator 1 Pediatrics
Chicago, IL $50,000.00-$65,000.00 5 months ago Chicago, IL $50,000.00-$65,000.00 1 month ago Chicago, IL $49,920.00-$81,619.20 1 week ago Chicago, IL $49,920.00-$81,619.20 1 month ago Chicago, IL $60,000.00-$75,000.00 5 months ago Chicago, IL $60,000.00-$75,000.00 1 month ago Oak Brook, IL $75,000.00-$85,000.00 5 hours ago Chicago, IL $60,000.00-$75,000.00 1 week ago Chicago, IL $51,346.00-$55,000.00 2 weeks ago Streeterville, IL $49,920.00-$81,619.20 1 month ago Streeterville, IL $49,920.00-$81,619.20 1 month ago Des Plaines - Clinical Research Coordinator
Chicago, IL $49,920.00-$81,619.20 1 month ago Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr