Global Regulatory Strategy Lead - IND/CTA Submissions

Arrowhead Pharmaceuticals, Inc.; Los Angeles (CA); On-site; USD 110,000 - 190,000; Full time

Job summary

Arrowhead Pharmaceuticals, Inc. is seeking a Regulatory Affairs professional to lead and coordinate global regulatory filings and strategies in the United States. You will drive regulatory plans aligned with development goals and partner with cross-functional teams to ensure timely, compliant submissions.

The role emphasizes managing IND/CTA submissions, communicating regulatory updates, and navigating FDA and international guidelines in a fast-paced, entrepreneurial environment.

Qualifications

• Lead and coordinate global regulatory filings and strategies.
• Ensure compliance with FDA and international guidelines.
• Manage IND/CTA submissions and communicate regulatory updates.

Skills

Regulatory affairs

IND submissions

FDA guidance

Job description

Arrowhead Pharmaceuticals, Inc. is seeking a Regulatory Affairs professional to lead and coordinate global regulatory filings and strategies in the United States. You will drive regulatory plans aligned with development goals and partner with cross-functional teams to ensure timely, compliant submissions.

The role emphasizes managing IND/CTA submissions, communicating regulatory updates, and navigating FDA and international guidelines in a fast-paced, entrepreneurial environment.