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, … Read more