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Clinical Research Coordinator II - Cancer Center
Posted Jul 28, 2026 · We last checked this listing on Oct 6, 2026
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Likely interview questions for this role
Written from this job description, not a generic list. Each one notes what the interviewer is really checking.
About your past
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.
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.
What would you do
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.
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.
A patient wants to leave a trial but feels guilty about letting the doctor down. How do you handle that conversation?
What they are checking: Whether they protect the patient's right to withdraw and handle the emotional side with care.
About the work
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.
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.
How do you get ready for a sponsor monitoring visit or an audit?
What they are checking: Whether their source documents and regulatory binders would hold up under outside review.
How have you helped manage a study budget or tracked billing for research procedures?
What they are checking: Whether they can keep research charges separate from standard care, which prevents billing errors for patients.
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Practice this out loudThe full job description
As published by Medical College of Wisconsin.
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