Future Opportunity: Site Monitor I/II - FSP - Single sponsor (Turkey)
Primary Location: Turkey, Remote ID de la oferta R0000035595 Categoría Clinical Trials Fecha de publicación 09/15/2025Overview
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
Future Opportunity: Site Monitor I/II - FSP - Single sponsor.
Are you passionate about making a difference and ready to take the next step in your career? While we may not have a live vacancy at the moment, we’re always looking to connect with talented individuals who are interested in joining our team in the near future.
If you're excited about the possibility of working with us, we encourage you to submit your details today. Let’s start the conversation now, so we’re ready when the right opportunity comes along.
Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is the space where today’s visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionize patients’ well-being. Every choice and step we make is guided by our unwavering focus on patients, fostering an environment where innovation thrives.
The Site Monitor will be responsible for data integrity, and data quality and ensuring 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.
Open to Clinical Research Associates with experience of 3 + years of
independent onsite monitoring, all types of visits.
Experience required:
• A minimum of 3 years experience as an oncology clinical monitor (CRA) with demonstrated experience of monitoring onsite in Turkey.
• Experience in managing complex protocols in Oncology or other therapeutic areas (TAs) where protocols are determined to be high risk:
• Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
• Experience in utilizing systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator Site File (eISF) (Florence)
We offer exceptional financial rewards, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.
Apply today!
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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 ProyectosExperto en la MateriaGestión de Proyectos
Perspectivas de los empleados
nuestro equipo
POR QUÉ TRABAJAR EN PAREXEL
