About ICF ICF (www.icf.com) is a consultancy firm with offices in the UK, Belgium, US and worldwide. At ICF, we help governments, public agencies and international institutions solve complex problems and improve the quality of life of people around the
Description Line Manager, Regulatory Affairs, EU remote, Spain, Poland or Germany, This role combines people leadership and operational delivery, actively contributing to the execution of clinical trial regulatory activities. As a Line Manager & Regulatory
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. We are more than one of the world’s leading
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
ICF (NASDAQ: ICFI) is a nearly $2 billion global solutions and technology services provider—but we’re not your typical consultants. With more than 9,000 employees across 70+ countries, we combine deep domain expertise with leading-edge technology to help
Consultant in the Health policy area We are looking for a Researcher/Consultant to join our well-established Policy in Action team, which provides evaluation, impact assessment and research services to European Commission Directorates-General. In particular, we are
About ICF (www.icf.com) is a consultancy firm with offices in the UK, Belgium, the US and worldwide. At ICF, we help governments, public agencies and international institutions solve complex problems and improve the quality of life of people around
The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. This role will be responsible
Role Barcelona onsite - 3 days office/ 2 days home. Join our Hematology R&D team at AstraZeneca, where we are committed to advancing the science to deliver life‑changing medicines to patients most in need. Our focus
Regulatory Affairs & Compliance Specialist basada en BARCELONA Habilidades, experiencia, cualificaciones. Si tiene el perfil adecuado para esta oportunidad, asegúrese de inscribirse hoy mismo. Desde LHH estamos apoyando a uno de nuestros clientes, entidad de investigación
In short Compruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación. Position: Junior Clinical Development Location: Azuqueca de Henares. Experience: 3
Hays is collaborating with an international pharmaceutical company specialized in the development, manufacturing, and commercialization of medicines , with a strong focus on generics and a solid commitment to R&D and clinical development . ¿Es este
Senior Consultant – EU Education and Training Policy – EU Consulting (research and programme implementation role) Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de
Description No deje pasar esta oportunidad, inscríbase rápidamente si su experiencia y habilidades coinciden con lo que se indica en la siguiente descripción. We are expanding our services and looking for a Consultant to join our
The La descripción completa del puesto cubre todas las habilidades asociadas, la experiencia previa y cualquier cualificación que se espera que tengan los solicitantes. Trial Delivery Leader (TDL) serves as the single point of accountability for
At Desplácese hacia abajo para encontrar los detalles completos de la oferta de trabajo, incluyendo la experiencia requerida y las funciones y tareas asociadas. ICF Next, we believe great impact starts with great people. You’ll join a
Hays is collaborating with an international pharmaceutical company specialized in the development, manufacturing, and commercialization of medicines , with a strong focus on generics and a solid commitment to R&D and clinical development . The project
Hays is collaborating with an international pharmaceutical company specialized in the development, manufacturing, and commercialization of medicines, with a strong focus on generics and a solid commitment to R&D and clinical development . ¿Quiere presentar una
Pivotal is excited to expand our team and we are looking for an experienced, highly motivated Quality Assurance Technician who shares our vision of providing clinical research excellence. Joining Pivotal as a Quality Assurance Technician means
Consultant – Health Policy Area No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. We are looking for a Researcher/Consultant to join our well‑established