Regulatory Affairs Associate

hace 3 semanas


Buenos Aires, Argentina Parexel A tiempo completo

Overview When our values align there’s no limit to what we can achieve. At Parexel we share the same goal—to improve the world’s health. From clinical trials to regulatory consulting and market access, every clinical development solution we provide is underpinned by a deep conviction in what we do. Each of us, no matter what we do, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, do it with empathy, and are committed to making a difference. Required Experience IC Key Skills Proofreading Adobe Acrobat FDA Regulations Manufacturing & Controls Biotechnology Clinical Trials Research & Development GLP cGMP Product Development Chemistry Writing Skills Employment Details Employment Type: Full-TimeExperience: yearsVacancy: 1 #J-18808-Ljbffr



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