Roles › Clinical Research Coordinator Center
Chicago, IL
Clinical Research Coordinator Center jobs in Chicago, IL
3 open roles from 1 employer. Checked Oct 6, 2026.
What these openings look like
All 3 are at Lurie Children's Hospital. Every one publishes a pay range, and they run $46,280 to $96,928 a year. Every posting is full time. The most recent went up on Oct 2, 2026.
Every listing links to the employer's own application. Nothing is posted here on their behalf, and nothing is reposted from anywhere else.
Open roles
Clinical Research Coordinator III-Center for Cancer and Blood Disorders
Posted Oct 2 · Verified Oct 6
Clinical Research Coordinator I-Center for Cancer and Blood Disorders
Posted Sep 16 · Verified Oct 6
Clinical Research Coordinator II-Center for Cancer and Blood Disorders
Posted Aug 19 · Verified Oct 6
What it pays here
Only some employers publish a range. These are the ones that did, as written in their own postings:
- $59,280–$96,928 a year
- $46,280–$75,670 a year
- $49,920–$81,619 a year
What they ask clinical research coordinator center candidates here
Drawn from the 3 open postings on this page. The ones that come up across several employers are near the top.
Walk me through what you do to prepare for a site initiation visit on a pediatric oncology trial.
What they are checking: Whether they know study start-up steps well enough to coordinate with minimal supervision.
How do you explain a research study to a parent whose child was just diagnosed with cancer?
What they are checking: Whether they can support informed consent and assent with compassion and without pressure.
What is the difference between consent and assent in pediatric research, and how do you document both?
What they are checking: Core knowledge of pediatric research ethics and regulatory requirements.
A sponsor monitor finds missing source documents during a visit. How do you respond?
What they are checking: Whether they handle findings honestly and fix the root cause, not just the single gap.
How do you keep a regulatory binder current across amendments, IRB approvals and staff changes?
What they are checking: Whether they maintain the regulatory documents the posting says they manage.
Tell me about a protocol deviation you were involved in. What happened and what changed afterward?
What they are checking: Whether they report deviations openly and help prevent repeats.
How do you report a serious adverse event, and what are the timelines you watch?
What they are checking: Whether they understand safety reporting rules that protect children in trials.
You are coordinating several studies and two have visits on the same day. How do you manage it?
What they are checking: Their organization and ability to balance study demands without errors.
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