Roles › Clinical Research Coordinator Cancer Center

Milwaukee, WI

Clinical Research Coordinator Cancer Center jobs in Milwaukee, WI

3 open roles from 1 employer. Checked Oct 6, 2026.

What these openings look like

All 3 are at Medical College of Wisconsin. None of these postings publish a pay range. Every posting is full time. The most recent went up on Sep 18, 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 I - Cancer Center

Medical College of Wisconsin · Milwaukee, WI · Full time

Posted Sep 18 · Verified Oct 6

Clinical Research Coordinator II - Cancer Center

Medical College of Wisconsin · Milwaukee, WI · Full time

Posted Sep 10 · Verified Oct 6

Clinical Research Coordinator II - Cancer Center

Medical College of Wisconsin · Milwaukee, WI · Full time

Posted Aug 13 · Verified Oct 6

What they ask clinical research coordinator cancer 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 how you obtain informed consent from a cancer patient for a clinical trial.

What they are checking: Whether they treat consent as an ongoing conversation that protects a vulnerable patient, not a signature to collect.

Tell me about the oncology trials you've coordinated and what phase they were in.

What they are checking: How much cancer trial experience they bring and whether they understand the different demands of each phase.

A patient on study has a serious adverse event over the weekend. What happens on Monday morning?

What they are checking: Whether they know SAE reporting timelines and who must be notified, which is a core compliance duty.

How do you screen a patient against complex eligibility criteria, and how do you document it?

What they are checking: Whether they are careful with inclusion and exclusion criteria, since enrolling an ineligible patient is a major deviation.

What's involved when you prepare an IRB submission or a protocol amendment?

What they are checking: Whether they know the IRB process in practice and can draft documents with the investigator.

You notice a required scan was done outside the protocol window. What do you do?

What they are checking: Whether they report deviations openly and fix the process, rather than hide them from the sponsor or PI.

How do you keep a study on track when appointments and procedures depend on several departments?

What they are checking: Whether they can coordinate across radiology, pharmacy and clinics so protocol timepoints are not missed.

Tell me about a time you trained or supervised someone on research procedures.

What they are checking: Whether they can teach and guide junior staff, since this role includes training and supervision.

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