20 Apr

Clinical Research Associate Willing Relocate Argentina Empleos vacantes en Pra Health Sciences

Position
Clinical Research Associate Willing Relocate Argentina
Company
Pra Health Sciences
Location
Opening
20 Apr, 2018 30+ days ago

Pra Health Sciences requiere con urgencia la posición de Clinical Research Associate Willing Relocate Argentina siguiente. Por favor, lea este anuncio de trabajo cuidadosamente antes de aplicar. Hay algunas calificaciones, experiencia y habilidades requisito de que los empleadores requieren. Hace tu trayectoria profesional encaja con estos requisitos? Asegúrese de que entiende el papel que está solicitando y que se adapta a sus habilidades y calificaciones.

Siga las instrucciones en línea, completar todos los campos necesarios, y proporcionar toda la información pertinente para que su solicitud sea presentada correctamente. Al hacer clic en el botón 'Apply this Job' (abre en ventana nueva) se le llevará al formulario de solicitud en línea. Aquí se le pedirá que proporcione datos personales y de contacto, responder a preguntas relacionadas con el empleo, y mostrar cómo usted cumple con los criterios de selección clave.

Clinical Research Associate Willing Relocate Argentina Empleos vacantes en Pra Health Sciences Empleos Detalles:

  • Clinical Research Associate 2 - Willing to relocate to Argentina

    Job Locations - | VE
    Posted Date 2 months ago(3/14/2018 4:03 PM)
    ID
    2018-45233

Overview

The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

Responsibilities

  • Applies knowledge of PRA’s policies and procedures
  • Demonstrates excellent written and oral communication
  • Demonstrates excellent knowledge of ICH/GCP
  • Displays ability to manage investigative sites to facilitate trial deliverables
  • Demonstrates ability to escalate issues appropriately
  • Conducts monitoring to confirm subject safety and data ntegrity
  • Describes and demonstrates the principals of IP accountability
  • Identifies scientific misconduct at the site level
  • Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms
  • Mentors CRAs new to the position or company
  • Serves as an observation visit leader
  • Conducts monitoring evaluation visits
  • Assists team lead in the development of trial tools or documents

Qualifications

  • Read, write and speak fluent English; fluent in host country language required.
  • 2+ years of clinical monitoring experience required
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
  • Clinical research experience
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • An advanced degree (e.g., M.S., M.B.A., PharmD, etc)
  • Experience in monitoring all trial components (PSSV to COV)
  • Experience in coaching/mentoring other CRAs

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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