Associate Director, Preclinical Subject Matter Expert, Regulatory Affairs and Drug Development Solutions

Job title: Associate Director, Preclinical Subject Matter Expert, Regulatory Affairs and Drug Development Solutions

Company: IQVIA

Job description: (CoE) within the Regulatory Affairs and Drug Delivery Solutions (RADDS) department. Prepares and/or reviews relevant… preclinical regulatory submissions to support clinical trial and marketing authorization activities for either internal…

Expected salary:

Location: Bangalore, Karnataka

Job date: Sat, 03 Jun 2023 04:43:55 GMT

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