Description 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
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
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
At ICF Next, we believe great impact starts with great people. You’ll join a diverse, multidisciplinary team working at the intersection of strategy, creativity, and public impact, delivering meaningful projects for EU institutions and public‑interest organisations. In
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
Solutia Life Sciences is the recruitment division of Solutia, specializing in technical and middle management roles within the pharmaceutical, biotech, and medical device sectors. We are currently supporting a clinical-stage biotech company in Barcelona in their
Updated: Yesterday Location: Madrid, Spain Job ID: Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum,
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
Estamos buscando un/a Project Finance Analyst para uno de nuestros clientes, una firma especializada en crecimiento empresarial y financiación estratégica para startups y pymes está ampliando su equipo de Funding. Buscamos una persona con mentalidad analítica,
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
Regulatory Affairs & Compliance Specialist basada en BARCELONA Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud. Desde LHH estamos apoyando a uno de nuestros clientes, entidad de investigación biomédica en
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
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 . The project
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
Responsabilitats Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto. Per a lanàlis d’operacions creditícies i de risc, cerquem ANALISTA DE RISCOS que tindrà com a principals funcions: Anàlisi
Responsibilities Si sus habilidades, experiencia y cualificaciones coinciden con las de esta descripción del puesto, no demore su solicitud. Assist/advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements