Rush University Medical Center
Senior Clinical Research Coordinator - Emergency Medicine-20736
Rush University Medical Center, Chicago, Illinois, United States, 60290
Senior Clinical Research Coordinator - Emergency Medicine-20736
Senior Clinical Research Coordinator - Emergency Medicine-20736
Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: ER Research Recruit - Corbin
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)
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 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 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. Master’s 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 study’s 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
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Senior Clinical Research Coordinator - Emergency Medicine-20736
Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: ER Research Recruit - Corbin
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)
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 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 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. Master’s 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 study’s 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
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Chicago, IL $117,520.00-$193,918.41 1 month ago Chicago, IL $122,000.00-$192,000.00 3 days ago Scientific Manager, COA Implementation, Patient Centered Solutions
Chicago, IL $95,300.00-$237,500.00 1 month ago Clinical Trial Manager - Central Midwest
Chicago, IL $95,000.00-$125,000.00 3 days ago Chicago, IL $63,079.00-$75,000.00 3 days ago Chicago, IL $145,000.00-$190,000.00 1 week ago Evanston, IL $56,782.00-$79,850.00 1 week ago Sr Manager Flow Cytometry Core Facility - Research Core - Full-time-21864
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Chicago, IL $130,800.00-$241,000.00 3 days ago Healthcare Clinical Legal Fellow (Postdoctoral Research Associate) - Department of Medicine
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Chicago, IL $50,000.00-$65,000.00 1 month ago Chicago, IL $49,920.00-$81,619.20 2 months ago Clinical Research Coordinator - Ophthalmology Clinic
Chicago, IL $49,920.00-$81,619.20 3 months 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