About The Position

IMA Clinical Research is hiring a full-time Clinical Research Coordinator in Chicago, Illinois, to support CNS and behavioral health clinical trials. The coordinator will guide participants through their study journeys and gain hands-on experience across the company’s Phase II–IV trial portfolio; the company does not conduct Phase I studies. The role supports day-to-day trial operations, participant coordination, study documentation, monitoring, regulatory reviews, safety reporting, and retention. The position offers a predictable schedule with no evenings, weekends, or on-call work.

Requirements

  • At least 2 years of experience coordinating clinical research studies.
  • Proficiency in phlebotomy.
  • Bachelor’s degree.
  • Ability to multitask across active studies.

Nice To Haves

  • CNS, psychiatry, psychology, neuroscience, or behavioral health research experience.
  • CCRC certification; it is not required.

Responsibilities

  • Run day-to-day trial operations, keeping studies on protocol and on track.
  • Coordinate scheduling, procedures, assessments, and follow-up visits.
  • Perform phlebotomy and handle specimen collection and processing.
  • Serve as a liaison between participants, investigators, sponsors, and CROs.
  • Maintain source documents and case report forms in audit-ready condition.
  • Support monitoring visits and regulatory reviews.
  • Assist with safety reporting and participant retention.

Benefits

  • Medical insurance.
  • Dental insurance.
  • Vision insurance.
  • 401(k) with employer match.
  • Paid time off (PTO).
  • Company holidays and a floating holiday.
  • Tuition reimbursement.
  • Student loan repayment assistance.
  • Paid parental leave.
  • Predictable schedule with no evenings, weekends, or on-call work.
  • Advancement paths in a growing CRO.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service