Clinical Research Nurse: Trials & IRB Lead

Indiana University

Indianapolis (IN)

On-site

USD 60,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Medical insurance
HSA
FSA
Tuition subsidy
Paid holidays

Job summary

Indiana University in Indianapolis is seeking a Research Nurse/Study Coordinator within the Department of Anesthesia. The role supports protocol development, risk assessment, recruitment, consent, and regulatory submissions for clinical studies.

Responsibilities include coordinating enrollment, liaising with health professionals, handling specimens, budgets, and audits, and coaching staff on GCP and study procedures.

Qualifications

  • Combination of related education and experience may be considered.
  • Education beyond minimum may substitute for work experience.
  • Work experience beyond minimum may substitute for education.

Responsibilities

  • Assists PI and participates in protocol development and risk assessment.
  • Designs recruitment strategies and consents subjects per IRB/protocol.
  • Recruits subjects and monitors enrollment goals.
  • Ensures proper collection, processing, and shipment of specimens; communicates with lab and sponsor.
  • Prepares study budgets and reconciles accounts; reviews contracts/agreements.
  • Submits IRB documents (consent, ads, protocol).
  • Schedules training and educates staff on study procedures and GCP.
  • Manages study inventory and maintains compliance docs.
  • Prepares for monitor visits and sponsor/FDA audits.
  • Keeps up-to-date with regulatory affairs and clinical literature.

Skills

Multitasking
Regulatory experience
Quality mindset
Financial data analysis
Interpersonal skills
Customer relationships

Education

Bachelors nursing +1y
Associate nursing +3y
High school+4y experience

Job description

Indiana University in Indianapolis is seeking a Research Nurse/Study Coordinator within the Department of Anesthesia. The role supports protocol development, risk assessment, recruitment, consent, and regulatory submissions for clinical studies.

Responsibilities include coordinating enrollment, liaising with health professionals, handling specimens, budgets, and audits, and coaching staff on GCP and study procedures.

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