Clinical Research Registered Nurse

Live Well Homecare Agency, LLC

Springfield (MO)

On-site

USD 55,000 - 75,000

Full time

2 days ago
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Job summary

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

Qualifications

  • 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.

Responsibilities

  • 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.

Skills

Nursing judgment
Informed consent
Regulatory knowledge
Documentation skills
Multidisciplinary collaboration

Job description

Clinical Research Nurse

to support and coordinate clinical trials within a Healthcare & Medical Services setting.



  • 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.


Key qualifications/skills:

Strong clinical nursing judgment, knowledge of informed consent and regulatory standards, meticulous documentation skills, and the ability to collaborate effectively in a multidisciplinary environment.

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