Visiting Clinical Research Coordinator

Last updated: August 17, 2026

Responsibilities

As part of this dynamic Cancer Center CTO team, Clinical Research Coordinators will manage & oversee several oncology clinical trials, from study inception to termination.

Responsibilities for this position include but are not limited to: activation & maintenance of the oncology clinical trials protocols; acting as liaison between physicians, clinic staff, UIC IRB office, sponsors, & regulatory agencies; educating physicians & clinic staff on impact of protocol modifications & adverse events; assisting physicians & clinic staff in identification, recruitment, and enrollment of patients for clinical trial protocols; planning & coordinating strategies for increasing patient enrollment at University and affiliate sites, acting as liaison between patients, physicians, & sponsors in patients’ enrollment compliance to regulations, especially FDA & NCI, and sponsor guidelines; reviewing protocols to ensure compliance with laboratory & clinic procedures & ensuring that evaluations are met; & providing expertise on clinical components regarding physician, patient, & clinic staff compliance.

Requirements

Bachelor’s degree in nursing (with current IL licensure to practice) plus 2 years clinical research experience required; oncology clinical research experience a plus. Proficiency with information systems & knowledge of federal regulations & guidelines regarding clinical trials preferred; SoCRA certification (or equivalent) a plus, and required within 2 years of hire. Requires excellent written, oral & interpersonal communication skills, as well as a strong ability to organize, prioritize, & coordinate multiple activities to meet deadlines. Experience with electronic medical records is desirable. Must be proficient in MS Office, including MS Access.

Scientific Case Review

Would you like to understand whether current clinical programs, recent research developments, or emerging approaches may be relevant to your individual situation?

Share your question with our scientific research team and receive information focused on the areas of current research that may be relevant to your case.

• Review of the information you provide
• Relevant research and clinical program information
• A clear response focused on your situation

What happens next? Send your question, receive a focused scientific review, and get a clear response about research and clinical programs relevant to your situation.

Your scientific review will be prepared by Dr. Helen Melnik, PhD , who has more than 25 years of experience in stem cell research and international clinical programs.

☎ WhatsApp Request My Personal Scientific Review ✉ Email Request My Personal Scientific Review

No obligation. Your question will be reviewed confidentially.

Educational and research information only. This service does not constitute medical advice, diagnosis, prescription, or a personalized treatment recommendation.