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Regulatory Affairs Sr. Manager/Associate Director in Pasadena, CA

Arrowhead Research

Pasadena, CA 91101
6w ago


Life Sciences


8 - 10 years

Job Description

The Position

The Global Regulatory Lead (GRL) is responsible for facilitating global drug product development and global registration by contributing to the development and execution of regulatory strategies and effective regulatory agency interactions. The GRL will be responsible for providing day to day regulatory support to the project team and regulatory team management.


  • Develop effective regulatory strategies for global submissions pertaining to specific projects to expedite the development, filing, and regulatory approval for new development products
  • Participate in product development teams to support execution of regulatory strategy ensuring regulatory deliverables are met within agreed upon timelines and provide appropriate advice and support to ensure compliance with all regulatory requirements
  • The GRL will also be the primary day-to-day liaison with th
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Valid through: 2020-3-4

About Arrowhead Pharmaceuticals

Arrowhead Research is a publicly traded (NASDAQ: ARWR) pharmaceutical company that is a component of the NASDAQ Biotechnology Index. As of 2016[update], it has no marketed products. Products in development are RNA therapeutics acting through RNA interference mechanisms of action. The company focuses on treatments for Hepatitis B, and Carcinomare. The company has six products in its pipeline, in various stages of clinical development. In 2015, the company substantially expanded its intellectual property holdings through complete acquisition of the full RNAi research and development portfolio and assets from Novartis.
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