Clinical Research Coordinator: Drive Impactful Trials

PRADEEP THAPAR MD SC

Orland Park (IL)

On-site

USD 45,000 - 65,000

Full time

9 days ago
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Benefits offered by this job

401(k)
Health insurance
Paid time off

Job summary

Premier Psychiatry in Orland Park, IL is seeking a dedicated Clinical Research Coordinator to join our team and advance medical research in a clinical setting. You will coordinate trial operations, screen and enroll participants, collect data, and ensure regulatory compliance with IRB, GCP, and FDA guidelines, serving as liaison among sponsors, investigators, and participants.

We value detail-oriented professionals with familiarity of EDC systems and medical record software; a bachelor's degree

Qualifications

  • Bachelor's degree in life sciences, healthcare, or related field preferred.
  • Experience in clinical research coordination or a clinical setting is a plus.
  • Familiarity with GCP, ICH guidelines, and IRB submission processes.
  • Strong attention to detail with excellent organizational and time-management skills.
  • ACRP or SOCRA certification (CCRC/CCRP) is a plus.

Responsibilities

  • Coordinate and manage day-to-day clinical trial operations and research study activities
  • Screen, enroll, and monitor patient participants per study protocols
  • Collect, record, and maintain accurate clinical data and research documentation
  • Ensure compliance with IRB regulations, GCP guidelines, and FDA requirements
  • Serve as a liaison between sponsors, investigators, and study participants
  • Prepare and submit regulatory documents, reports, and study amendments
  • Schedule and coordinate study visits, procedures, and follow-up appointments

Skills

Attention to detail
Communication skills
Time management

Education

Bachelor's degree in life sciences/healthcare

Tools

EDC systems
Medical record software

Job description

Premier Psychiatry in Orland Park, IL is seeking a dedicated Clinical Research Coordinator to join our team and advance medical research in a clinical setting. You will coordinate trial operations, screen and enroll participants, collect data, and ensure regulatory compliance with IRB, GCP, and FDA guidelines, serving as liaison among sponsors, investigators, and participants.

We value detail-oriented professionals with familiarity of EDC systems and medical record software; a bachelor's degree

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