TRABAJO REGULATORY AFFAIRS CLINICAL WRITING BARCELONA, BARCELONA
(16 ofertas de trabajo)
Listado de trabajos de Regulatory affairs clinical writing en Barcelona, Barcelona
Global development scientist associate director/director
P rovide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... understanding of scientific and...
Global development scientist associate director/director
Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... understanding of scientific and clinical...
clinical operations, pharmacovigilance, medical affairs)... educating clinical staff on regulatory requirements, quality standards and good practices...
Global safety program lead (senior director)
clinical development, medical affairs, regulatory affairs)... experience of global regulatory submissions and interacting with major regulatory agencies...
Health, safety and quality section head (ref. ad/)
Oversee the facility's biosafety management, ensuring adherence to established protocols, regulatory compliance, and promotion of a safe working environment...
Medical safety lead / sr medical safety lead (crm)
regulatory compliance... skills: clinical trials... experience in clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing...
Senior manager, safety scientist
Authors high quality aggregate safety reports to meet regulatory and internal deadlines; ensures all safety regulatory documents are processed and submitted according...
Scientifical lead the interaction with regulatory authorities into therapeutical area... lead medical assessment for potential new candidates to enter a clinical...
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...
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Conduct endotoxin testing and bioburden assessments in compliance with regulatory requirements... fluent in spanish with basic to intermediate english communication...
Global practice area lead for biocides
Biology, chemistry, biochemistry, pharmacology) with a minimum of 10 years of experience in biocides regulatory affairs... excellent communicative skills in english...
Market surveillance specialist (temporary position)
Experience in providing demonstrations and writing technical reports... internal networking directly relationship with regulatory affairs, quality control, marketing...
Associate – life sciences consulting with medical evidence practice - madrid & barcelona
Iqvia is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries...
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