Clinical Research Nurse: Lead Trials and Patient Care

IU Health; Lafayette (IN); Vor Ort; USD 75.000 - 110.000; Vollzeit

Benefits dieser Stelle

401k match

Tuition reimbursement

Student loan forgiveness

Employee Assistance Program

Wellness program

Growth opportunities

Zusammenfassung

IU Health Arnett Hospital in Indiana is seeking a Clinical Research Nurse to blend direct patient care with oversight of clinical trials across inpatient and outpatient settings. You will screen, enroll, and assess participants while ensuring safety and regulatory compliance.

The role collaborates with physicians and sponsors, coordinates study activities, educates patients, and collects study data including phlebotomy and IV placement.

Qualifikationen

• ASN required; BSN preferred.
• Active RN license in Indiana or NLC RN license.
• Graduated from a nationally accredited nursing program.
• 5–7 years of relevant nursing experience.
• BLS certification by the American Heart Association (AHA).
• Other advanced life support certifications may be required per unit/department.
• Knowledge of FDA regulations governing clinical trials.
• Ability to perform physical assessments.
• Phlebotomy skills to draw blood and start IVs.
• Proficiency in Microsoft Office applications.

Aufgaben

• Screen, recruit, and enroll patients into clinical studies.
• Conduct study visits and patient assessments.
• Coordinate study activities and regulatory requirements.
• Collaborate with physicians, sponsors, and interdisciplinary teams.
• Educate patients and families about research participation.
• Collect study data and perform research procedures including phlebotomy and IV placement.

Kenntnisse

Clinical nursing

Phlebotomy

IV placement

Regulatory compliance

MS Office proficiency

Ausbildung

ASN (Associates of Nursing)

BSN preferred

Tools

Microsoft Office

Jobbeschreibung

IU Health Arnett Hospital in Indiana is seeking a Clinical Research Nurse to blend direct patient care with oversight of clinical trials across inpatient and outpatient settings. You will screen, enroll, and assess participants while ensuring safety and regulatory compliance.

The role collaborates with physicians and sponsors, coordinates study activities, educates patients, and collects study data including phlebotomy and IV placement.