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... resolution of safety questions from regulatory authorities, investigators, internal development teams, ... operations, translational research, clinical pharmacology, regulatory affairs, quality assurance, biostatistics, data ... of safety input to key..
... for the position of Clinical Regulatory Affairs Manager. Primary responsibilities include ... Primary responsibilities include implementing global regulatory strategies with managerial oversight, independently ... support preparation and maintenance of..
u00A0Who We AreFor more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were founded ..
BioMarinu2019s Research & Development group is responsible for everything from research and discovery to post-market clinical development. Research & Development involves all bench and clinical research and the associated groups that ..
... finance, legal, human resources, corporate compliance and ethics, and information technology. ... description The Supply Chain Security Specialist will play a key role ... and associated risk management and..
Who We Are For more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were ..
... finance, legal, human resources, corporate compliance and ethics, and information technology. ... lives. The Supply Chain Security Specialist will play a key role ... and associated risk management and..
u00A0BioMarin Pharmaceutical Inc. is a company founded in 1997 and based in San Rafael, CA that specializes in the development of therapeutics for serious and often times life-threatening rare diseases, in ..
... handled in accordance with global/local regulatory requirements and company policiesResponsible for ... MRPs and PSPs to ensure compliance with PV requirements/regulationsRaises or increases ... the PV Operations team on..
... science/technology and the trend of regulatory requirements. Contributes to regulatory interactions with regulatory authorities such as FDA as ... status quo for improvements in compliance with appropriate regulatory requirements...