Orthopaedics Health Services Research Analyst – Onsite

Montgomery College

Nashville (TN)

Presencial

USD 65.000 - 90.000

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

Vanderbilt Health in Nashville is seeking a Health Services Research Analyst to support NIH-funded studies within the Department of Orthopaedic Surgery. This on-site role involves enrolling participants, maintaining study protocols, IRB submissions, and coordinating with investigators and clinical teams.

You will work with a team to ensure compliance with Good Clinical Practice and sponsor guidelines, manage data, and report progress in weekly meetings.

Formación

  • Bachelor’s Degree (or equivalent experience).
  • Minimum of 2 years of relevant experience; 2–5 years preferred.
  • Ongoing access to reliable transportation.
  • Experience in REDCap is a plus.

Responsabilidades

  • Maintain accurate and timely documentation of study procedures and communication with investigators and federal sponsors.
  • Maintain IRB documentation and ensure research is conducted in accordance with Good Clinical Practice Guidelines and sponsor guidelines.
  • Recruit appropriate individuals for study participation according to study protocol, which involves medical chart review, physician and/or community outreach, and patient screening or interviewing.
  • Enroll eligible study participants.
  • Communicate regularly with investigators and other members of the research team on ongoing study protocols.
  • Attend weekly research team meetings.
  • Prepare data reports.
  • Maintain study database.

Conocimientos

Study Design
Research Admin
Data Management
Data Analysis
Presentation

Educación

Bachelor's Degree

Herramientas

REDCap

Descripción del empleo

Vanderbilt Health in Nashville is seeking a Health Services Research Analyst to support NIH-funded studies within the Department of Orthopaedic Surgery. This on-site role involves enrolling participants, maintaining study protocols, IRB submissions, and coordinating with investigators and clinical teams.

You will work with a team to ensure compliance with Good Clinical Practice and sponsor guidelines, manage data, and report progress in weekly meetings.

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