skip to main content

Important Notice

It appears you are using an older version of your browser. While some functions will be available, IllinoisJobLink.com works best with a modern browser such as the ones provided by:

Please download and install the latest version of the browser of your choice. We apologize for any inconvenience.



Behavioral Research Coordinator II-Telemedicine

Click the Facebook, Google+ or LinkedIn icons to share this job with your friends or contacts. Click the Twitter icon to tweet this job to your followers. Click the link button to view the URL of the job, which then can be copied and pasted into an e-mail or other document.

Job Details
Job Order Number
6975259
Company Name
Ann & Robert H. Lurie Children's Hospital of Chica
Physical Address
225 E Chicago Ave # # 14
Chicago, IL 60611
Job Description

Job LocationsUS-IL-Chicago
Behavioral Research Coordinator II-Telemedicine

Requisition ID
2019-10828

Category
Research

Position Type
Regular Full-Time

Shift
Days

Overview

Coordinates all clinical research activities with moderate supervision.
Responsibilities

1. Conducts quality assurance activities.

2. Conducts study start-up activities and prepares and maintains all regulatory documents required by sponsor and/or regulatory agencies.

3. Prepares protocols, informed consent documents, modifications, renewals and other necessary documents for review by the IRB and/or sponsor and trains staff on protocol/procedures.

4. Coordinates study conduct with other departments to effectively implement behavioral research projects; obtains required letters of support and/or approvals as needed (i.e., IBC, SRC, etc.) and protocol is followed.

5. Identifies and recruits eligible study subjects; conducts informed consent/assent process.

6. Arranges and conducts behavioral research visits including delivering behavioral interventions when appropriate.

7. Attends appropriate research meetings.

8. Abstracts data from medical records and enters medical information/data onto protocol specific case report forms, study flow sheets, and other required study forms; prepares abstracted/coded data for processing/analysis.

9. Coordinates reimbursement of subjects.

10. Collects specimens from subjects and processes specimens or works with Research lab to ensure samples are processed/sent out correctly when appropriate.

11. Records data on source documents and CRFs and/or electronic web based systems.

12. Monitors/assesses adverse events and reports them as required.

13. Adheres to research protocol in compliance with applicable institutional, local and federal regulations (OHRP, FDA, GCP, etc.).

14. Functions as participant liaison for study questions, billing issues, etc.

15. Maintains all study documents (regulatory binders, source documents, correspondence, etc.).

16. Promotes the ethical conduct of research by actively participating in research related educational meetings/conferences.

17. Performs job functions adhering to service principles with customer service focus of innovation, service excellence and teamwork to provide the highest quality care and service to our patients.

18. QA/QC checks for database validity and data monitoring.

19. Tracking deadlines for grants/deliverables.

20. Conducts statistical analysis under PI supervision.

21. Other job functions as assigned.
Qualifications

1. Bachelor* s degree in a related field preferred. A combination of education and/or experience may be considered in lieu of the degree when the experience is dirctly related to the duties of the job.

2. Minimum of 3 to 5 years of experience in behavioral program or research required.

3. Knowledge of research regulations preferred.

4. Good clinical practices documentation required.

5. Familiarity and experience with IRB regulatory requirements preferred.

EEO/AA Employer/Vets/Disability


To view full details and how to apply, please login or create a Job Seeker account.