Clinical Research Nurse: Lead Patient-Centered Trials

Mercy Co

Clayton (MO)

Presencial

USD 70.000 - 95.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

Mercy Research is seeking a Clinical Research Nurse to coordinate and manage clinical trials, ensuring patient safety, regulatory compliance, and accurate data collection across Mercy’s research program.

The CRN will serve as a liaison among participants, physicians, sponsors, CROs, and the research team while supporting staff training and a growing portfolio of studies. Strong nursing background and communication skills are essential.

Formación

  • RN license in the applicable state.
  • Nursing degree: RN with BSN/ ADN/ Diploma.
  • 2+ years (BSN) or 3+ years (ADN/Diploma) nursing experience.
  • Ability to perform patient assessments and clinical procedures.
  • Strong communication, organization, and teamwork skills.
  • Proficiency with Microsoft Office and electronic systems.

Responsabilidades

  • Coordinate and manage assigned clinical trials from study start-up through completion.
  • Conduct study feasibility assessments and support study initiation activities.
  • Maintain thorough knowledge of study protocols and ensure compliance with all research requirements.
  • Administer or oversee investigational medications, treatments, and procedures as outlined in study protocols.
  • Apply clinical judgment to support patient care, protocol adherence, and research operations.
  • Screen, consent, educate, and enroll research participants.
  • Perform patient assessments and monitor participants throughout study participation.
  • Collect vital signs, ECGs, spirometry, blood glucose readings, and other study-related assessments.
  • Monitor for adverse events and ensure participant safety at all times.
  • Schedule and coordinate research visits while maintaining a positive participant experience.
  • Accurately collect, document, and maintain clinical research data and source documentation.
  • Complete case report forms and research records in a timely manner.
  • Collect and process laboratory specimens as required by study protocols.
  • Maintain study supplies, equipment, and investigational product inventories.
  • Ensure compliance with ICH/GCP guidelines, federal regulations, and institutional policies.
  • Participate in quality assurance, monitoring visits, and audit activities.
  • Partner with physicians, nurses, clinical staff, sponsors, and CROs to ensure successful study execution.
  • Assist in training, mentoring, and precepting new research team members.
  • Support research assistants, office staff, and volunteers.
  • Foster a collaborative, professional, and patient-focused research environment.
  • Assist with participant recruitment initiatives and study awareness efforts.
  • Serve as a liaison between Mercy Research, sponsors, and community partners.
  • Attend investigator meetings and research-related training opportunities, including occasional travel as needed.

Conocimientos

Communication skills
Organizational skills
Analytical skills
Problem-solving
Multitasking

Educación

Nursing Diploma
ADN
BSN

Herramientas

Microsoft Office
Electronic systems

Descripción del empleo

Mercy Research is seeking a Clinical Research Nurse to coordinate and manage clinical trials, ensuring patient safety, regulatory compliance, and accurate data collection across Mercy’s research program.

The CRN will serve as a liaison among participants, physicians, sponsors, CROs, and the research team while supporting staff training and a growing portfolio of studies. Strong nursing background and communication skills are essential.

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