Eu Regulatory Submissions Lead

Viatris seeks a Senior Specialist, Electronic Submissions to support end-to-end publishing and submission of regulatory dossiers for new and existing products. You will ensure quality control, electronic transmission, and archiving, while mentoring junior colleagues and leading publishing activities.This international role requires strong English...

Assegurar o acompanhamento estratégico da regulação e políticas públicas com impacto nos negócios da Repsol em Portugal. Identificar riscos e oportunidades, coordenar respostas e elaborar documentos técnicos.

IQVIA Inc. is seeking a Regulatory Affairs Specialist to join its Biotech Regulatory Affairs team in Lisbon. You will support clinical development programs, focusing on EU CTR submissions and regulatory compliance across Europe.The role requires hands-on EU CTR submission experience, strong regulatory knowledge, and collaboration with global project teams to...

IQVIA Inc. is seeking a Regulatory Affairs professional to join our Biotech Regulatory Affairs team in Lisbon, Portugal. You will support EUCTR submissions and provide regulatory guidance across European clinical research programs, including chemical entities and biologics.You will work with a global project-based team to ensure timely, compliant regulatory...

IQVIA Inc seeks a Principal Medical Writer to develop regulatory documents for submissions to global regulatory authorities, including IBs, CSRs, and MA submissions. You will provide strategic direction to cross-functional teams and lead the writing of complex, data-driven clinical manuscripts to ensure accuracy and regulatory compliance.You will oversee...

A Jobgether procura um Manager, Regulatory Affairs baseado em Portugal para liderar atividades regulatórias em mercados internacionais. A função exige comunicação eficaz com equipas multifuncionais e stakeholders globais.Você irá supervisionar submissões a agências regulatórias e comitês de ética, orientar equipes em conformidade com ICH GCP e...

Procure outros empregosDescrição do cargoRegulatory professional to manage EU CTIS submissions, clinical trial applications, and regulatory documentation for study start-up.Criar um alerta de emprego para esta pesquisaEmpregos similaresProject Lead in Portugal for Clinical Trial Services (CTS) projects, focusing on client relationships, project delivery,...

IQVIA is seeking a Principal Medical Writer to lead the development of regulatory documents for global submissions. You will provide strategic direction to cross-functional teams and oversee multiple compounds, ensuring data is presented accurately and clearly according to regulatory standards.The role requires a strong background in biopharmaceutical...

Viatris is seeking a Regulatory Strategy Lead to drive EU regulatory strategy across a diverse medicinal product portfolio. You will lead submissions, ensure compliance, and coordinate with internal teams to align regulatory requirements with business goals. Required: pharmacy/biotech background, 5+ years RA, fluent English, and strong interpersonal skills....