Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our
ABOUT HOLCIM+ CONCRETE Holcim+Concrete is part of Holcim+, the global digital platform that integrates and enhances all customer-facing applications across Holcims diverse business lines (Cement, Aggregates, Ready-Mix Concrete, and Solutions & Products). It serves as a
Are you an experienced full service Project Director in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology. Are you passionate about impacting the
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our
Are you an experienced full service Project Director in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology. Are you passionate about impacting the
Global Sr CTM - Home Based in SPAIN. FSP. Oncology experience is required. Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across
Responsible to coordinate the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM processes, standards, and technology. Member of the Global Study Team (GST) and the main point of
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
The University Hospital Vall dHebron is highly specialised in rare diseases at the regional, national, and international level, with its incorporation as a full member of 20 of the 24 European Reference Networks (ERNs). The scientific
Are you ready to orchestrate complex, global oncology studies that accelerate lifesaving medicines to patients? In this role, you will connect scientific ambition with disciplined execution, ensuring pivotal trials move from protocol to meaningful results with
TFS HealthScience invites a Freelance Clinical Database Programming Process Lead to join our CDS Group Management team. Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen
Salary Range:63,600.00 - 118,000.00Job Description Summary#LI-HybridLocation: Barcelona, SpainAs Associate Director - Clinical Data Analytics and Technology, you will help build and lead a new Barcelona-based team shaping the next generation of clinical data capabilities at Novartis. This
WHY CHOOSE MEDSIR ¿Es este el puesto que está buscando? Si es así, siga leyendo para obtener más detalles y no olvide enviar su solicitud hoy mismo. We are a Barcelona-based fastest-growing company founded by scientific
Job Title: Senior Clinical Programmer ILocation: BarcelonaAt AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality.
About Evinova Evinova enables global life sciences to accelerate better health outcomes through innovative digital health solutions for clinical research.Role Overview Evinova is seeking an entrepreneurial, AI-fluent Product Director to take ownership of a core product
We are seeking an experienced project professional to join our Operations team in Spain, supporting international observational field studies and secondary data studies. We welcome applications from Senior Project Associates acting as Project Managers, Clinical Project
Overview As Principal Clinical Data Standards Consultant, you provide expert-level standards knowledge and shape ICONs standards content for internal and sponsor-facing projects. You will develop and maintain standards libraries compliant with CDISC and regulatory requirements, guiding
Overview As Principal Clinical Data Standards Consultant, you provide expert-level standards knowledge and shape ICONs standards content for internal and sponsor-facing projects. You will develop and maintain standards libraries compliant with CDISC and regulatory requirements, guiding
Overview Recuerde revisar su CV antes de enviar la solicitud. Además, asegúrese de leer todos los requisitos relacionados con este puesto. In this role you will oversee site management, clinical and central monitoring to safeguard patient