TRABAJO REGULATORY AFFAIRS ASSOCIATE STUDY BARCELONA, BARCELONA
(15 ofertas de trabajo)
Listado de trabajos de Regulatory affairs associate study en Barcelona, Barcelona
Response documents, study protocols, psrs, etc... • identify regulatory risks and propose mitigations to lead rpm and cross-functional teams...
Global development scientist associate director/director
P rovide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... the global development scientist...
Global development scientist associate director/director
Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... the global development scientist associate...
Global study manager, cell therapy
Support the global study associate director (gsad) in project management... monitor study conduct and progress, resolving risks and issues impacting study delivery...
Associate director, biostatistics
This is what you will do: the associate director, biostatistics has sufficient experience working as a statistician in the pharmaceutical industry to independently...
Associate clinical development director (oncology)
London, basel or barcelona role type: hybrid working, #li-hybrid the associate clinical development director (oncology) (assoc... clinical trial protocols (ctps)...
Associate director, global health economics & outcomes research
Partnering with heor product lead to develop heor tactical and clinical development plans that will provide a competitive advantage to differentiated payer evidence...
Associate director, global health economics & outcomes research
Medical research & development regulatory commercial etc... partnering with heor product lead to develop heor tactical and clinical development plans that will provide...
Medical affairs statistician lead
Provide expert input on study protocols and methodological strategy... stay current on regulatory and methodological developments and promote best practices...
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Associate director solution architect
We are looking for an experienced individual in global drug development regulatory affairs to lead technical activities for the solutions that re-define how novartis...
Educating clinical staff on regulatory requirements, quality standards and good practices... support regulatory inspections (fda, ema), including preparation, hosting...
Global safety program lead (senior director)
Experience of global regulatory submissions and interacting with major regulatory agencies... clinical development, medical affairs, regulatory affairs)...
We are currently seeking an in-house clinical research associate (ihcra) to join our diverse and dynamic team... what you will be doing assisting in the planning...
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¿Quieres encontrar trabajo?