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bristol-myers squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.one shared journey is moving us forward at bristol-myers squibb. .....
bristol-myers squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.one shared journey is moving us forward at bristol-myers squibb. .....
bristol-myers squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.one shared journey is moving us forward at bristol-myers squibb. .....
ionis Pharmaceuticals, inc., located in the north san diego county city of carlsbad, was founded in 1989 to create advanced, novel medicines to treat diseases with an unmet medical need. we are the pioneer and Leader in the Discovery and development .....
the position position scopeprogram Director is the core individual contributor position for commercial Regulatory Affairs (cora) review.incumbents in this position: lead program review committees (prcs) independently demonstrate mastery of the .....
main responsibilities:responsibility for developing a comprehensive registration Strategy in close cooperation with the personnel dealing with Sales, Operations, Vaccines and Marketing, taking into consideration company's interests and normative .....
for current gilead employees and contractors: please log onto your internal Career site to apply for this job. job description gilead Sciences, inc. is a Research-based biopharmaceutical company that discovers, develops and commercializes innovative .....
requisition id: reg004122position overview- basic functions & responsibility this position achieves company objectives, in line withcompany goals, through the submission and management of regulatory submissionsto Health authorities in australia .....
provides regulatory expertise and guidance to Clinical, global Drug Safety, legal, scientific, commercial, and other internal stakeholders for successful development of company core data sheets (ccdss) and global labeling, i.e., us and eu (cp, mrp, .....
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