Clinical Research Nurse: Trials Coordinator & Patient Care

Live Well Homecare Agency, LLC; Springfield (MO); Presencial; USD 55.000 - 75.000; Jornada completa

Descripción de la vacante

Live Well Homecare Agency, LLC seeks a Clinical Research Nurse to support and coordinate trials within a Healthcare & Medical Services setting. Responsibilities include managing study protocols, ensuring regulatory compliance, and obtaining informed consent while providing compassionate, patient-centered care.

This role requires meticulous documentation and collaboration with physicians, coordinators, and multidisciplinary teams to advance trial outcomes and quality improvement across

Formación

• Strong clinical nursing judgment and knowledge of regulatory standards.
• Meticulous documentation skills throughout study conduct.
• Ability to collaborate effectively in a multidisciplinary environment.
• Familiarity with informed consent processes and participant safety.
• Experience coordinating clinical research activities and data collection.

Responsabilidades

• Manage study protocols and ensure adherence to required research procedures.
• Maintain regulatory compliance and support ethical conduct of trials.
• Obtain informed consent and provide compassionate, patient-centered care.
• Collect, verify, and accurately document clinical research data.
• Coordinate with physicians, clinical research coordinators, and multidisciplinary teams across specialties.
• Communicate participant needs and trial updates to the broader care and research team.
• Contribute to continuous learning and quality improvement in clinical research practices.

Conocimientos

Nursing judgment

Informed consent

Regulatory knowledge

Documentation skills

Multidisciplinary collaboration

Descripción del empleo

Live Well Homecare Agency, LLC seeks a Clinical Research Nurse to support and coordinate trials within a Healthcare & Medical Services setting. Responsibilities include managing study protocols, ensuring regulatory compliance, and obtaining informed consent while providing compassionate, patient-centered care.

This role requires meticulous documentation and collaboration with physicians, coordinators, and multidisciplinary teams to advance trial outcomes and quality improvement across