LAVORO RESPONSABILE REGULATORY AFFAIRS PARMA, EMILIA ROMAGNA
(19 offerte di lavoro)
Listado de trabajos de Responsabile regulatory affairs en Parma, Emilia romagna
Senior global regulatory affairs project manager
Experience required 5 years in regulatory with good knowledge of drug development and regulatory procedures education at least bachelor’s degree in life sciences...
Responsabile sviluppo prodotti elettromedicali
· collaborerai con marketing, quality, operations e regulatory affairs per garantire che le specifiche tecniche siano allineate alle esigenze del mercato e alle...
Responsabile sviluppo prodotti elettromedicali (ann401783)
· collaborerai con marketing, quality, operations e regulatory affairs per garantire che le specifiche tecniche siano allineate alle esigenze del mercato...
regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...
Senior clinical research physician non-obstructive respiratory diseases
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... collaborate with clinical program leaders, statisticians, regulatory...
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... engage with regulatory authorities, external experts, and key...
Clinical research physician copd/bronchiectasis
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... outstanding communication skills with ability to interact with...
Stay current with regulatory guidelines and industry trends related to patient engagement and innovation in clinical research... act as the main point of contact...
Principal extractable and leachable scientist
Stay updated with the latest industry trends and regulatory changes... support to commercial manufacturing division in answering questions from regulatory...
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Head of clinical project management
Ensure cpms maintain compliance with internal sops, gcp, and regulatory standards... strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements...
Modeling & simulation scientist
Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...
Global r&d demand and business knowledge data scientist
It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery...
Scopo il/la local master data specialist è responsabile della gestione e manutenzione dei dati master a livello di plant produttivo di san leonardo, assicurando...
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