Clinical Research Coordinator - Cardiology/Pediatrics
- Tracking Code
- 3866-177
- Job Description
- General Summary of Position Responsibility:Collects and manages patient and laboratory data for clinical research projects. Screens and oversees the recruitment of subjects.Essential Job Functions:
- Arrange study visits and provides instructions.
- Assists in creating and updating case report forms and/or source documents.
- Abstracts data from medical records and enters medical information/data onto protocol specific case reports forms, study flow sheets and other required study forms.
- Assists in identifying eligible subjects.
- Creates and performs QA/QC procedures, orders supplies for data collection, develops worksheets/tools for collecting patient data and enters data electronically via web based systems.
- Assists with preparation of protocols, informed consents, amendments and other necessary documents for review by the IRB and sponsor.
- Prepares abstracted/coded data for computer processing/analysis. Attends investigator meetings.
- Processes specimens.
- Maintains investigator/sponsor files in accordance with FDA and Good Clinical Practice (GCP) Guidelines.
- 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, families, co-workers and others.
Knowledge, Skills and Abilities:- Bachelor ‘s degree required, preferably in a related field, with either 1-3 years experience in clinical researchOr Minimum of 1 year experience as a Clinical Research Associate.
- Familiarity and experience with FDA and IRB regulatory requirements is preferred.
- Job Location
- Chicago, Illinois, United States
- Position Type
- Full-Time/Regular
FTE Status
1.0
Work Days
Mon - Fri
Shift Hours
8:00am - 5:00pm
Shift
DAY
