Clinical Research Coordinator II — Oncology Trials Specialist

University of Chicago

United States

On-site

USD 60,000 - 75,000

Full time

14 days+
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Benefits offered by this job

Health benefits
Retirement plan
Paid time off

Job summary

The University of Chicago is seeking a Clinical Research Coordinator II to support, coordinate, and independently manage daily clinical trial activities under PI direction. You will help with compliance, data management, and study operations across hematology and oncology projects.

The role requires 2–5 years in clinical research, a college degree, and strong collaboration with sponsors, CROs, and regulatory authorities to ensure protocol adherence and patient safety.

Qualifications

  • Education: college/university degree in related field.
  • 2-5 years of work experience in a related job discipline.
  • Preferred: Bachelor’s degree and clinical research experience.

Responsibilities

  • Manages all aspects of conducting clinical trials including screening, enrollment, subject follow-up, CRF completion, and adverse event reports.
  • Recruits and interviews potential study patients with guidance from PI.
  • Collects, processes, ships and stores specimens according to aseptic techniques.
  • Coordinate startup through closeout including informed consent and protocol adherence.
  • Plan and coordinate patient schedules for study procedures and visits.
  • Educate patients about procedures, visit schedules, and risks/benefits.

Skills

Clinical research coordination
Regulatory compliance
IRB submissions

Education

Bachelor’s degree

Job description

The University of Chicago is seeking a Clinical Research Coordinator II to support, coordinate, and independently manage daily clinical trial activities under PI direction. You will help with compliance, data management, and study operations across hematology and oncology projects.

The role requires 2–5 years in clinical research, a college degree, and strong collaboration with sponsors, CROs, and regulatory authorities to ensure protocol adherence and patient safety.

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