Site Monitor - FSP - Spain

Parexel; Cantabria; A distancia; EUR 35.000 - 55.000; Jornada completa

Descripción de la vacante

Una empresa innovadora busca un Monitor de Sitio para unirse a su equipo de operaciones clínicas en España. Esta es una oportunidad única para trabajar con uno de los 10 principales grupos farmacéuticos del mundo, enfocándose en estudios de oncología que tienen un impacto real. Con la flexibilidad de trabajar desde casa y menos carga de trabajo, podrás mantener un equilibrio saludable entre tu vida laboral y personal. Además, recibirás formación adaptada a tu experiencia, lo que te permitirá crecer profesionalmente mientras contribuyes a proyectos significativos. ¡Únete a nosotros y marca la diferencia!

Formación

• 3 años de experiencia en monitoreo de sitios de forma independiente.
• Conocimiento de ICH GCP y excelente gestión del tiempo.

Responsabilidades

• Configurar y supervisar estudios, completar informes de estado.
• Participar en la presentación de protocolos y documentos de consentimiento.

Conocimientos

Gestión del tiempo

Habilidades sociales

Atención al detalle

Conocimiento de ICH GCP

Educación

Licenciatura en ciencias de la vida o disciplina relacionada

Descripción del empleo

Do you know why we are one of only three CROs to have received the Leadership Award for 11 consecutive years? Because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do.

Join our team and develop your career with us by contributing your personal and professional talents and skills. Together we will continue to do things that matter to people.

Parexel FSP is looking for a Site Monitor in Spain (Madrid or Barcelona) to strengthen our clinical operations team. Work from home and with the flexibility you want. Our SMs have less travel and less workload to maintain work-life balance. We offer long-term projects, world-class technology and training tailored to your individual experience.

As a SM, you will work independently and will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. You will participate in the submission of protocols, consent documents for ethics / IRB approval and assist in the preparation of regulatory submissions as requested.

You will have the opportunity to be a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact.

Minimum Requirements:

• Bachelor's degree in a life science or related discipline.
• Minimum of 3 years' experience in independent site monitoring - all types of visits.
• Understanding of ICH GCP Compliance.
• Excellent time management and social skills.
• Highly motivated with a phenomenal eye for detail.
• Ability to travel domestically and internationally approximately 65%-75% of working time. Expected travelling ~2-3 days / week.

Send me your updated resume for an immediate interview.