Clinical Research Nurse - Study Coordination & Patient Care

Northwestern Medicine

Chicago (IL)

On-site

USD 85,000 - 110,000

Full time

4 days ago
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Job summary

Northwestern Medicine is seeking a Clinical Research Nurse in Chicago to support investigator-initiated and sponsor trials. The CRN will serve as a liaison between NU investigator teams and Northwestern Medical Group, ensuring compliant study conduct throughout the protocol lifecycle.

The role requires an RN license, a bachelor’s degree (or equivalent), and 2 years of clinical research trial experience, with strong communication, organizational, and computer skills.

Qualifications

  • Bachelor’s degree or equivalent experience is required.
  • Licensed as a Registered Nurse is required.
  • Two years’ experience managing all aspects of clinical research trials.
  • Intermediate computer and internet knowledge.
  • Excellent customer service and patient care skills.
  • Meticulous organizational and communication abilities.

Responsibilities

  • Facilitates and coordinates logistical aspects of study protocols with research staff.
  • Provides direct nursing patient care including admissions, medications, and study-related tests.
  • Represents the protocol team at meetings and site visits with investigators and monitor vendors.
  • Ensures accurate data entry and documentation related to study subjects and events.
  • Trains staff and maintains study files and regulatory communications.

Skills

Communication skills
Patient care
Organizational skills
Interpersonal skills
Basic computing
Clinical research knowledge

Education

Bachelor's degree or equivalent experience
Master's degree in Nursing

Job description

Northwestern Medicine is seeking a Clinical Research Nurse in Chicago to support investigator-initiated and sponsor trials. The CRN will serve as a liaison between NU investigator teams and Northwestern Medical Group, ensuring compliant study conduct throughout the protocol lifecycle.

The role requires an RN license, a bachelor’s degree (or equivalent), and 2 years of clinical research trial experience, with strong communication, organizational, and computer skills.

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