Clinical Research Coordinator

Chicago, IL - USA

Monthly Salary: Not Disclosed

Posted on: 11 days ago

Vacancies: 1 Vacancy

Job Summary

Job Summary

Our clinical research team has an immediate need at our Chicago office for an experienced Clinical Research Coordinator who is familiar with managing clinical pharmaceutical and device protocols. The ideal candidate will be organized and willing to work a problem to its successful completion. Previous experience in ICH guidelines IBR requirements and sponsor research organization protocols is preferred.

Responsibilities and Duties

Represents Illinois Research (IR) in a professional and courteous manner (verbal written and in appearance) when interacting with Illinois Research staff sponsors IRBs and subjects.
Must be moral and ethical in decision making and during interaction with patients sponsor and IRB representatives physicians and other staff.
Able to independently manage workflow.
Maintains ongoing communication with Director of Research Associate Director of Research Principal Investigator/Sub-Investigator other study personnel and sponsor/CRO per IR SOPs and as deemed necessary.
Possesses a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.
Maintains confidentiality of patient and/or protocol issues as appropriate and as bound by Confidentiality Agreements with IR between IR and sponsors and between IR and other entities.
Is creative and diligent in the recruitment of qualified study subjects into assigned protocols to fulfill enrollment obligations within the sponsors timeline while following all policies and regulations governing medical ethics IRB requirements federal regulations/ICH guidelines GCPs and IRs SOPs.
Has training certificate in and competently perform pediatric/adult phlebotomy.
Obtains blood and urine samples and then processes and ships specimens as required.
Able to accomplish protocol specified patient visits and procedures.
Clearly and concisely documents patient assessments observations test results and other study related information per federal regulations/ICH guidelines GCPs IR SOPs sponsor/CRO and IRB requirements.
Maintains accurate and complete written source documentation of patient visits and protocol related activities.
Accurately completes CRFs/eCRFs and/or worksheets generated by the sponsor/CRO within 1 to 3 business days of the subjects visit.
Maintains subject screening logs and protocol deviation logs.
Responds to monitor notes and/or emails in a timely manner.
Accounts for clinical trial materials (i.e. CRFs study drug lab supplies and/or other required items) and ensures availability of appropriate amounts for the conduct of the study.
Attends required training courses/conferences in order to stay abreast of current and changing federal regulations and AICR policies.
Attends Investigator Meetings as directed.
Performs all duties in a safe and prudent manner.
Promptly reports adverse events to Associate Director of Research Principal

Qualifications and Skills

Associate or Bachelors Degree preferred
At least two (2) years of previous research and/or clinical experience is required
Bilingual a plus

Benefits

Illinois Research offers a competitive benefits package to eligible employees. Below are some of the benefits you may receive as an employee at AICR.

Collaborative work culture
Medical Dental and Vision Insurance
Voluntary Short Disability
401(k) with Employer Match
Paid Time Off (PTO)
Group Term Life Insurance
Health Care & Dependent Care Flexible Spending Accounts
Competitive Wages
Paid Holidays

Illinois Research is an Equal Opportunity Employer

Required Experience:

Job SummaryOur clinical research team has an immediate need at our Chicago office for an experienced Clinical Research Coordinator who is familiar with managing clinical pharmaceutical and device protocols. The ideal candidate will be organized and willing to work a problem to its successful complet...

Job Summary

Responsibilities and Duties

Represents Illinois Research (IR) in a professional and courteous manner (verbal written and in appearance) when interacting with Illinois Research staff sponsors IRBs and subjects.
Must be moral and ethical in decision making and during interaction with patients sponsor and IRB representatives physicians and other staff.
Able to independently manage workflow.
Maintains ongoing communication with Director of Research Associate Director of Research Principal Investigator/Sub-Investigator other study personnel and sponsor/CRO per IR SOPs and as deemed necessary.
Possesses a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.
Maintains confidentiality of patient and/or protocol issues as appropriate and as bound by Confidentiality Agreements with IR between IR and sponsors and between IR and other entities.
Is creative and diligent in the recruitment of qualified study subjects into assigned protocols to fulfill enrollment obligations within the sponsors timeline while following all policies and regulations governing medical ethics IRB requirements federal regulations/ICH guidelines GCPs and IRs SOPs.
Has training certificate in and competently perform pediatric/adult phlebotomy.
Obtains blood and urine samples and then processes and ships specimens as required.
Able to accomplish protocol specified patient visits and procedures.
Clearly and concisely documents patient assessments observations test results and other study related information per federal regulations/ICH guidelines GCPs IR SOPs sponsor/CRO and IRB requirements.
Maintains accurate and complete written source documentation of patient visits and protocol related activities.
Accurately completes CRFs/eCRFs and/or worksheets generated by the sponsor/CRO within 1 to 3 business days of the subjects visit.
Maintains subject screening logs and protocol deviation logs.
Responds to monitor notes and/or emails in a timely manner.
Accounts for clinical trial materials (i.e. CRFs study drug lab supplies and/or other required items) and ensures availability of appropriate amounts for the conduct of the study.
Attends required training courses/conferences in order to stay abreast of current and changing federal regulations and AICR policies.
Attends Investigator Meetings as directed.
Performs all duties in a safe and prudent manner.
Promptly reports adverse events to Associate Director of Research Principal