Clinical Research Coordinator at Illinois Cancercare
Peoria, IL 61615, USA -
Full Time


Start Date

Immediate

Expiry Date

30 Oct, 25

Salary

27.0

Posted On

30 Jul, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Numbers, Office Equipment, Dexterity

Industry

Hospital/Health Care

Description

Overview:
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.

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.
Responsibilities
  • 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.
    Qualifications:
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