LAVORO REGULATORY CLINICAL TRIAL SUBMISSIONS PARMA, EMILIA ROMAGNA
(7 offerte di lavoro)
Listado de trabajos de Regulatory clinical trial submissions en Parma, Emilia romagna
Senior clinical research physician non-obstructive respiratory diseases
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... clinical section of the investigator’s brochure, protocols and clinical...
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... the cpl ensures scientific and medical integrity in the development...
Head of clinical project management
Strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements, and cro/vendor management... experience required at least 8–10 years of experience...
Senior global regulatory affairs project manager
Ensure overall gra project timelines are aligned cross-ta / cross-functional teams and support the coordination of timely regulatory submissions...
regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...
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