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Clinical Site Monitor I or II - FSP Oncology/Turkey

Türkiye, Remote ID de la oferta R0000022353 Categoría Clinical Trials Fecha de publicación 05/01/2024
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Overview

Como Auxiliar de investigación clínica (CRA) en Parexel, usted cumple una función vital para hacerles llegar los tratamientos a los pacientes con mayor rapidez. La prioridad de nuestros CRA es la seguridad y el bienestar de los pacientes. Cuando viaje a centros de investigación y cumpla sus obligaciones de monitoreo, lo alentamos a ser inquisitivo, a asumir responsabilidades, a construir relaciones y a actuar con integridad.

Únase a un equipo con una gran variedad de experiencias y conocimientos y trabaje en proyectos globales dentro de una amplia gama de áreas terapéuticas. Estamos buscando personas que deseen crecer en el ámbito personal y profesional y que respalden a sus colegas de manera global y multidisciplinaria.

Perfil del éxito

¿Posee estas competencias sociales y rasgos interpersonales para tener éxito en Parexel?

  • Comunicador
  • Organizado
  • Contratos laborales flexibles
  • Emprendedor
  • Orientado al detalle
  • Solucionador de problemas

Acerca de este rol

Parexel FSP is seeking Home-based Clinical Site Monitors/CRA I or II for

home-based positions.

Our sponsor is a global biopharmaceutical company dedicated to relentlessly seeking breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is a space where visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionize patients’ well-being. Every decision we make and every action we take is guided by our unwavering focus on patients, fostering an environment where innovation thrives.

The Site Monitor is responsible for ensuring data integrity, data quality, and compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan (SMP) and will be performed virtually for most activities to supplement on-site visit requirements.

The Site Monitor will collaborate with the Site Manager to ensure that the site follows the protocol and is inspection-ready and will coordinate with institutions and investigators at the local level.

Required Experience:

  • A minimum of 1 year of experience as a Clinical Research Associate with demonstrated experience in monitoring (virtual or onsite).

  • Site activation experience

  • Feasibility and site management experience.

  • CRO oversight experience

  • Submissions experience (will not be submitting as part of this role).

  • Experience in utilizing systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator Site File (eISF) (Florence)

  • Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience

We offer exceptional financial rewards, training, and development opportunities. You can expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.

Don’t miss this opportunity. Apply today!

#LI-TA1


#LI-REMOTE

POTENCIAL TRAYECTORIA PROFESIONAL

Parexel ofrece diversas trayectorias profesionales y programas de desarrollo interno para que los CRA avancen al próximo nivel. Esto podría incluir mejorar su puesto técnico, transferencia a gerencia o cambiar a otras áreas del negocio.

  • APEX CRA
  • CRA I
  • CRA II
  • CRA Sénior
  • Gestión de Proyectos
    Experto en la Materia
    Gestión de Proyectos

Perspectivas de los empleados

nuestro equipo

Female employee leaning on desk with Parexel logo in background Team photo
Larger team photo
Female employee with characters from an amusement park Female employee posing for a photo with beautiful landscape in the background
Team outing at laser tag Male employee with medical mask on sitting at desk with laptop open Team photo in an office setting

POR QUÉ TRABAJAR EN PAREXEL

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