Clinical Research Coordinator

At Illinois CancerCare, research is a core value and a vital part of our mission to provide cutting-edge cancer care. With over 13,000 patients enrolled in clinical trials over the past 40 years, our nationally recognized research program offers access to innovative therapies close to home.

As a Clinical Research Coordinator, you'll support physician investigators and guide patients through every step of their clinical trial journey, from screening and enrollment to treatment and follow-up. You'll be part of a collaborative team advancing cancer care through meaningful research.

This is a meaningful opportunity for someone passionate about advancing medical research and improving patient outcomes through clinical innovation.

Pay & Benefits

• Starting pay: $27.00 per hour
  (Based on experience, education, and other factors)
• Medical, dental, and vision insurance (multiple plan options)
• Special wellness programs - Maven, HingeHealth, Livongo, Vitality, and Wondr
• 401(k) retirement plan with employer contributions
• Company-paid life, short-term, and long-term disability insurance
• Health Savings Account (HSA) & Flexible Spending Accounts (FSA)
• Paid time off and holidays
• Employee Assistance Program (EAP)
• Discounts through our Perks Program

What You'll Do

• Collaborate with physicians and patients to screen, enroll, and manage participants in clinical trials.
• Ensure strict adherence to protocol requirements throughout the patient's participation.
• Assemble, monitor, and submit research data accurately and on time.
• Maintain and organize protocol binders and source documents.
• Communicate effectively with internal teams, external facilities, and patients.
• Support compliance with regulatory standards and contribute to quality control efforts.
• Perform additional duties as requested to support research operations.

What We're Looking For

• Bachelor's degree in a science or healthcare field required
• 3+ years of experience in a medical setting preferred
• Strong attention to detail and excellent communication skills
• Familiarity with clinical research protocols and documentation
• SoCRA or ACRP certification preferred

Work Environment & Physical Requirements

• Work is performed in both office and clinical settings, with occasional visits to local hospitals.
• Frequent interaction with physicians, staff, and patients is required.
• Requires full range of body motion including bending, lifting (up to 50 lbs), manual and finger dexterity, and eye-hand coordination.
• Must be able to distinguish and transcribe letters and numbers accurately.
• Requires use of standard office equipment including telephone, copier, fax machine, scanner, and computer.
• May involve working under stressful conditions or irregular hours.
• Work may be repetitive and occasionally high-stress, especially when managing time-sensitive tasks.
• Contact may involve dealing with upset or emotionally distressed individuals.