Clinical Research Nurse - Trials & Recruitment Lead

Indiana University; Indianapolis (IN); Presencial; USD 76.000 - 86.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Comprehensive medical and dental保险

Health savings account with IU terms

Paid holidays and winter break

Descripción de la vacante

Indiana University in Indianapolis is seeking a Research Nurse/Coordinator to support the Principal Investigator in protocol development, risk assessment, and study design evaluation. You will design recruitment strategies, consent participants, and monitor enrollment per IRB-approved methods.

You will liaise with healthcare providers to optimize recruitment, manage specimen handling and documentation, and support audits, while maintaining regulatory knowledge and GCP compliance.

Formación

• Proven ability to manage multiple priorities in a regulated setting.
• Strong understanding of clinical research norms and GCP.
• Experience interpreting financial data related to study budgets.
• Excellent written and oral communication with diverse teams.

Responsabilidades

• Assist PI with protocol development, risk assessment, and study design evaluation.
• Design and implement recruitment strategies; consent subjects and monitor enrollment.
• Coordinate with healthcare providers to optimize recruitment and enrollment.
• Ensure proper specimen handling, documentation, and communications with labs, PI, and sponsor.
• Review and manage study budgets; reconcile accounts and review contracts/agreements.
• Prepare IRB documents and support ongoing regulatory submissions.

Conocimientos

Multi-tasking

Regulatory compliance

Analytical thinking

Communication skills

Interpersonal skills

Client relationship building

Educación

Bachelor's degree in nursing

Associate's degree in nursing

High school diploma + LPN + 4 years experience

Descripción del empleo

Indiana University in Indianapolis is seeking a Research Nurse/Coordinator to support the Principal Investigator in protocol development, risk assessment, and study design evaluation. You will design recruitment strategies, consent participants, and monitor enrollment per IRB-approved methods.

You will liaise with healthcare providers to optimize recruitment, manage specimen handling and documentation, and support audits, while maintaining regulatory knowledge and GCP compliance.