Rush University Medical Center
Clinical Research Coordinator - Cancer Center - Aurora, IL-21162
Rush University Medical Center, Chicago, Illinois, United States, 60290
Overview
Clinical Research Coordinator - Cancer Center - Aurora, IL-21162 at
Rush University Medical Center . Location: Aurora, 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) After an initial training period, this position will be located in Aurora, IL at Rush Copley Medical Center. Training will take place on-site at the Chicago, IL Rush University Medical Center campus. Rush offers exceptional rewards and benefits; details at the Rush benefits page. Pay Range: $27.47 - $38.81 per hour Rush salaries are determined by many factors including education, job-related experience and skills, internal equity and market data. Offers may vary depending on the circumstances of each case. Summary
The position supports 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). The coordinator will manage multiple and/or complex clinical research studies conducted by PI(s), which may include grant-funded, industry-sponsored, and investigator-initiated studies. S/he will independently coordinate the implementation and execution of study protocols and perform a variety of study-related duties. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures. Required Job Qualifications
Bachelor\'s degree and 4 years of clinical research experience OR 8 years of clinical research experience. 3 years coordinating Human Subjects research. Advanced knowledge of Good Clinical Practices and Good Documentation Practices. Knowledge of current NIH and/or FDA regulations and guidelines related to clinical research. Strong project management skills including ability to meet deadlines and coordinate multiple aspects of the ongoing project. Problem-solving, critical decision making and professional judgement. Strong analytical and organizational skills with high attention to detail. 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 convey complex concepts to multiple audiences. Ability to collaborate within multi-disciplinary team settings. Availability to work evenings, overnight and weekends if called for under study protocols. Travel may be required. Preferred Job Qualifications
Bachelor’s degree in Sciences or health-related discipline. Relevant certification strongly preferred (CCRP, CCRA, CCRC, CIP). Responsibilities
Coordinate all aspects of the study including recruitment, consent, screening, scheduling, tracking and provide study updates to participants throughout the conduct of the study. Collect and enter data into study case report forms and/or electronic data capture system; respond to queries in a timely manner. Submit or partner with a regulatory coordinator to submit study-related documents, protocols and amendments to the IRB per policy and procedure. Ensure procedural documentation is accurate, complete, and in compliance with institutional, local, state and federal guidelines and regulations related to clinical research. May collect, process and ship potentially biohazardous specimens. May administer more complex structured tests and questionnaires per study protocols; may utilize study-related technology and equipment as part of assessment procedures. Provide ongoing study status updates; respond to questions and may create summary reports for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance during the conduct of the study. Organize and participate in auditing and monitoring visits. Report unanticipated problems (protocol deviations, adverse events, and serious adverse events). Partner with PI(s), sponsor, compliance, clinical staff and manager to identify and improve more complex processes as they relate to the conduct of the research study. May provide oversight, training and coaching to less experienced staff. 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
Mid-Senior level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
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Clinical Research Coordinator - Cancer Center - Aurora, IL-21162 at
Rush University Medical Center . Location: Aurora, 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) After an initial training period, this position will be located in Aurora, IL at Rush Copley Medical Center. Training will take place on-site at the Chicago, IL Rush University Medical Center campus. Rush offers exceptional rewards and benefits; details at the Rush benefits page. Pay Range: $27.47 - $38.81 per hour Rush salaries are determined by many factors including education, job-related experience and skills, internal equity and market data. Offers may vary depending on the circumstances of each case. Summary
The position supports 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). The coordinator will manage multiple and/or complex clinical research studies conducted by PI(s), which may include grant-funded, industry-sponsored, and investigator-initiated studies. S/he will independently coordinate the implementation and execution of study protocols and perform a variety of study-related duties. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures. Required Job Qualifications
Bachelor\'s degree and 4 years of clinical research experience OR 8 years of clinical research experience. 3 years coordinating Human Subjects research. Advanced knowledge of Good Clinical Practices and Good Documentation Practices. Knowledge of current NIH and/or FDA regulations and guidelines related to clinical research. Strong project management skills including ability to meet deadlines and coordinate multiple aspects of the ongoing project. Problem-solving, critical decision making and professional judgement. Strong analytical and organizational skills with high attention to detail. 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 convey complex concepts to multiple audiences. Ability to collaborate within multi-disciplinary team settings. Availability to work evenings, overnight and weekends if called for under study protocols. Travel may be required. Preferred Job Qualifications
Bachelor’s degree in Sciences or health-related discipline. Relevant certification strongly preferred (CCRP, CCRA, CCRC, CIP). Responsibilities
Coordinate all aspects of the study including recruitment, consent, screening, scheduling, tracking and provide study updates to participants throughout the conduct of the study. Collect and enter data into study case report forms and/or electronic data capture system; respond to queries in a timely manner. Submit or partner with a regulatory coordinator to submit study-related documents, protocols and amendments to the IRB per policy and procedure. Ensure procedural documentation is accurate, complete, and in compliance with institutional, local, state and federal guidelines and regulations related to clinical research. May collect, process and ship potentially biohazardous specimens. May administer more complex structured tests and questionnaires per study protocols; may utilize study-related technology and equipment as part of assessment procedures. Provide ongoing study status updates; respond to questions and may create summary reports for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance during the conduct of the study. Organize and participate in auditing and monitoring visits. Report unanticipated problems (protocol deviations, adverse events, and serious adverse events). Partner with PI(s), sponsor, compliance, clinical staff and manager to identify and improve more complex processes as they relate to the conduct of the research study. May provide oversight, training and coaching to less experienced staff. 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
Mid-Senior level Employment type
Full-time 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 . End of Refined Listing.
#J-18808-Ljbffr