Clinical Research Nurse Coordinator — On‑Call Study Liaison

Northwestern Medicine

Chicago (IL)

On-site

USD 85,000 - 110,000

Full time

14 days+
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Job summary

Northwestern Medicine is seeking a Clinical Research Nurse Coordinator in Chicago to join a multidisciplinary research team. The role requires ongoing collaboration with principal investigators and cross-functional staff to ensure compliant, efficient execution of clinical trials throughout study lifecycles.

The successful candidate will bring an Illinois RN license, 2+ years of clinical experience, and experience coordinating research protocols.

Qualifications

  • Current license as a Registered Nurse in Illinois.
  • Experience in clinical trials.
  • BSN degree.
  • Minimum of two years related clinical experience.
  • CPR-BLS Certification through the AHA.

Responsibilities

  • Leads the coordination and support to Principal Investigator(s).
  • Reviews research studies in pre-submission phase for feasibility of protocol implementation.
  • Guides the review, revision, and maintenance of protocols to meet compliance and regulatory requirements.
  • Provides guidance to clinical research nurses on projects related to new research submissions and workflows.
  • Develops and maintains clinical nursing research policies, SOPs, and guidelines.
  • Escalates research-related concerns to the appropriate leader or committee.
  • Mentors and collaborates with investigator teams and clinical/research staff.
  • Supports nursing staff during adverse events and emergencies.

Skills

Clinical trials
RN licensure (Illinois)
Two years clinical experience
CPR-BLS

Education

BSN
MSN

Job description

Northwestern Medicine is seeking a Clinical Research Nurse Coordinator in Chicago to join a multidisciplinary research team. The role requires ongoing collaboration with principal investigators and cross-functional staff to ensure compliant, efficient execution of clinical trials throughout study lifecycles.

The successful candidate will bring an Illinois RN license, 2+ years of clinical experience, and experience coordinating research protocols.

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