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Research Coordinator-Infectious Disease

Job in Evanston, Cook County, Illinois, 60208, USA
Listing for: Endeavor Health
Full Time, Part Time position
Listed on 2026-01-30
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 24.86 - 37.29 USD Hourly USD 24.86 37.29 HOUR
Job Description & How to Apply Below

Hourly Pay Range: $24.86 - $37.29 – The hourly pay rate offered is determined by a candidate's expertise and years of experience, among other factors.

Position Highlights
  • Position: Research Coordinator – Infectious Disease
  • Location: Evanston & Skokie, IL – other sites may be required
  • Full Time/Part Time: Full Time
  • Hours: Monday-Friday
  • Required Travel: Possible travel to study start‑up meetings
What you will do
  • Excellent interpersonal skills and the ability to interact in a professional and sensitive manner handling financial information, research project information, research proposals, and IRB paperwork.
  • Excellent organizational skills and attention to detail.
  • Computer literacy in Microsoft Word, Excel, and PowerPoint.
  • Familiarity with clinical data is preferable.
  • Provides clinical care services including consenting, treating, and monitoring patients.
  • Recruit and screen candidates for clinical trials.
  • Acquire past medical and medication history profiles.
  • Ship lab samples.
  • Dispense research drug to patients according to protocol.
  • Utilize electronic capture to update patient information.
  • Help to oversee clinical data for audits and oversight visits.
  • Perform a variety of research, data entry and regulatory duties of a routine and technical nature related to departmental research endeavors.
  • Ensure adherence to protocols and quality of information received.
  • Identifying and screening study participants, enrolling subjects to the trials in adherence with the protocol.
  • Assist with budget proposals and study budget tracking.
  • Assist with study time reporting.
  • Ensure compliance with local, state and Federal regulations for the protection of human subjects.
  • Complete regulatory submissions/revisions for the Institutional Review Board (IRB).
  • Communicate and coordinate with physicians, division staff, and other departmental study personnel as required for study design, implementation and completion.
  • Complete data abstraction and data entry for study‑specific databases.
  • Review and timely report study related adverse events to the sponsor.
What you will need
  • Bachelor’s degree required, in the fields of social, biological or healthcare sciences preferred.
  • 1-5 years of research experience.
  • Experience with phlebotomy, ECG and pharmacy practices preferred.
Benefits
  • Career Pathways to Promote Professional Growth and Development.
  • Various Medical, Dental, Pet and Vision options.
  • Tuition Reimbursement.
  • Free Parking at designated locations.
  • Wellness Program Savings Plan.
  • Health Savings Account Options.
  • Retirement Options with Company Match.
  • Paid Time Off and Holiday Pay.
  • Community Involvement Opportunities.

EOE:
Race/Color/Sex/Sexual Orientation/ Gender Identity/Religion/National Origin/Disability/Vets – VEVRRA Federal Contractor.

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