Clinical Study Coordinator
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- Coordinación de visitas de pacientes y gestión del estudio (site management)
- Introducción y validación de datos en eCRF
- Gestión documental (ISF, consentimientos informados, etc.)
- Interacción con CRAs y equipo investigador
- Cumplimiento de GCP y protocolo ¿Qué buscamos?
- Experiencia en clinical trials (Study Coordinator o Data Entry)
- Conocimiento de ICH-GCP
- Nivel de inglés medio-alto
- Perfil organizado, proactivo y detallista ¿Qué ofrecemos?
- Contrato de 18 meses
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Salario:
57.000€ brutos (por la totalidad del tiempo)
- Proyecto internacional fase III
- Excelente ambiente de trabajo
- Desarrollo y aprendizaje continuo Si quieres seguir creciendo en investigación clínica, nos encantará conocerte COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter
- Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.
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