Somos una asociación sin ánimo de lucro creada en 1994. Los socios de GEIS, médicos de muy diferente ámbito (oncólogos, patólogos, radioterapeutas, radiólogos, traumatóloglos, cirujanos, biólogos, etc.), trabajamos juntos para proporcionar formación en la patología del sarcoma, así como para fomentar la investigación clínica y pre-clínica.
GEIS participa en el desarrollo de avances para el manejo de los sarcomas y en la gestión de los estudios y ensayos clínicos que lleva a cabo como promotor o como colaborador de otros grupos y consorcios.
GEIS realiza cursos, máster propio en sarcomas, workshops específicos y un simposio internacional anual.
Colaboramos con asociaciones de pacientes.
Barcelona, Madrid, Sevilla, Zaragoza
2 Jun.
GEIS participa en el desarrollo de avances para el manejo de los sarcomas y en la gestión de los estudios y ensayos clínicos que lleva a cabo como promotor o como colaborador de otros grupos y consorcios.
GEIS realiza cursos, máster propio en sarcomas, workshops específicos y un simposio internacional anual.
Colaboramos con asociaciones de pacientes.
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Descripción • Perform site visits and monitor activities in accordance with protocol, GCP/ICH Guidelines, and applicable regulatory requirements, from SIV to SCV (phase I-IV)
• Mentor CRAs on monitoring, collaborate on procedures development, and query resolution.
• Review and verify case report forms and other clinical data for completeness and accuracy.
• Generate queries and manage resolutions with site staff.
• Maintain project tracking systems as required.
• Use expertise to identify and resolve complex site issues and deficiencies in documentation, communication, and the need for additional training.
• Identify protocol deviations or major risks to data integrity.
• Provide recommendations regarding site-specific actions.
• Act as a liaison between the company and study site personnel and be able to respond to site concerns and questions.
• IMP supply and control.
• Remote work will be approximately 90% of the time.
Descripción • Perform site visits and monitor activities in accordance with protocol, GCP/ICH Guidelines, and applicable regulatory requirements, from SIV to SCV (phase I-IV)
• Mentor CRAs on monitoring, collaborate on procedures development, and query resolution.
• Review and verify case report forms and other clinical data for completeness and accuracy.
• Generate queries and manage resolutions with site staff.
• Maintain project tracking systems as required.
• Use expertise to identify and resolve complex site issues and deficiencies in documentation, communication, and the need for additional training.
• Identify protocol deviations or major risks to data integrity.
• Provide recommendations regarding site-specific actions.
• Act as a liaison between the company and study site personnel and be able to respond to site concerns and questions.
• IMP supply and control.
• Remote work will be approximately 90% of the time.
Número de vacantes:
1
Modalidad de trabajo:
Full remoto (100%)
Tipo de contrato:
Full time.
Remuneración anual:
1.800€ nett/month
Ventajas sociales o económicas
Annual bonus, depending on objectives.
"
Requisitos
• Bachelor's degree in Science or equivalent combination of education, training and experience.
• Prior 1 year of clinical monitoring experience (preferably in Oncology).
• Fluency in English.
• Excellent communication, presentation, interpersonal skills, both written and spoken.
• Prior 1 year of clinical monitoring experience (preferably in Oncology).
• Fluency in English.
• Excellent communication, presentation, interpersonal skills, both written and spoken.
Áreas terapéuticas
Oncología
Habilidades
Ordenada y organizadaCapacidad multitareahabilidades de comunicación y relación interpersonalesestablecer prioridades
Estudios mínimos
Diplomado en Ciencias de la Salud
Idiomas
Inglés nivel Alto.
Experiencia mínima
1 año
Disponibilidad para viajar
El 60% del tiempo laboral