LAVORO GLOBAL REGULATORY AFFAIRS PHARMA PARMA, EMILIA ROMAGNA
(17 offerte di lavoro)
Listado de trabajos de Global regulatory affairs pharma en Parma, Emilia romagna
Senior global regulatory affairs project manager
Support internal initiative(s) with a goal to accelerate internal regulatory processes and subsequently development timeline - in collaboration with the gra global...
Chiesi corporate functions these are the functions supporting the business: global hr global finance, procurement & it group legal & corporate affairs global...
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...
Engage with regulatory authorities, external experts, and key stakeholders to shape development plans and ensure compliance with global regulatory requirements...
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... 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... it is divided into integrated functional...
Principal extractable and leachable scientist
Stay updated with the latest industry trends and regulatory changes... it is divided into integrated functional areas focusing on pipeline projects including...
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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...
Chiesi global manufacturing division chiesi group has four production plants: parma (italy), the strategic hub for the production and distribution of our products...
Vuoi trovare lavoro?
Vuoi trovare lavoro?
