Responsabilidadesproject plan development and control.project documents development (protocol, pis, investigator and central trial master files, etc.).collaboration in the development and validation of ecrfs.start-up process management including finance and legal aspects.project control: documents, study procedures, imp, monitoring, and financing.preparation of documents for internal and external audits/inspections.elaboration, delivery, and control of project reports.biological samples shipment management and control.remote monitoring of observational studies.collaboration in project data management.requisitosuniversity degree in life sciences.knowledge and experience in clinical trials development.high english level (c1, advanced or similar).previous experience in health sciences.habilidadesattention to detail.organization and time management.computer tools proficiency.administrative work.ability to work independently or in a team.communication oral and written.estudios mínimosdiploma (or similar).idiomasenglish, level alto.disponibilidadavailability to travel.20% of the working time.modalidad de trabajohybrid (50% in office, 50% remote).tipo de contratocontract until maternity leave.ventajas sociales o económicasapprox.€ netos / mes.#j-*-ljbffr