Clinical Research Coordinator
- Hematology/Oncology
- Chicago (Lincoln Park)
- Full time
- Days
Position Summary:
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.
FTE status: FT-80
Requirements
Knowledge,
skills and abilities:
· Bachelor’s
degree required, preferably in a related field, with 1-3 years experience in
clinical research
-OR-
· Minimum
of 1 year experience as a CRC I with increased responsibility; has been or is
capable of performing the majority of CRC II responsibilities.
· Familiarity
and experience with FDA and IRB regulatory requirements is preferred.