LAVORO QUALITY REGULATORY AFFAIRS MEDICAL PARMA, EMILIA ROMAGNA
(21 offerte di lavoro)
Listado de trabajos de Quality regulatory affairs medical 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...
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...
Clinical research physician copd/bronchiectasis
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... they ensure scientific and medical integrity in the development and...
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... engage with regulatory authorities, external experts, and key...
Stay current with regulatory guidelines and industry trends related to patient engagement and innovation in clinical research... we strive to enhance patients’ well-being...
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...
Intern - commercial business partner china & international
Support and collaborate with multiple teams such as data analytics, sales, operations, marketing, and medical affairs on project requirements, timelines, adjustments...
Modeling & simulation scientist
Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...
Vuoi trovare lavoro?
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...
Sr. director, r&d external opportunities
It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery...
Intern - global value and access - pricing jr analyst
Air and care franchises are also supported by the medical affairs, value & access, and business excellence & customer experience global functions...
Due diligence lead - temporary
) and facilitates the transition from dd to deal signature and post-deal handover to the future project leadership team experience required experience gained in...
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...
Vuoi trovare lavoro?
Vuoi trovare lavoro?