Global Regulatory Affairs Manager — Submissions & Strategy

Arrowhead Pharmaceuticals; San Diego (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

Arrowhead Pharmaceuticals, Inc. seeks a dynamic Regulatory Affairs professional to support multiple global regulatory projects, ensuring compliance with applicable requirements and developing regulatory plans.

You will report to the Director, Regulatory Affairs and work with cross‑functional teams to align strategies and submissions. The role focuses on IND/CTA/IMPD filings, health authority interactions, and global submissions, with opportunities to influence product development and

Qualifications

• Experience in regulatory affairs for pharma/biotech products.
• Ability to contribute to regulatory strategies and submissions.
• Excellent communication with health authorities and internal teams.

Responsibilities

• Support global regulatory projects and plans.
• Assist with IND/CTA/IMPD filings and health authority interactions.
• Collaborate with cross-functional teams to align regulatory strategies.

Skills

Regulatory affairs

IND/CTA/IMPD filings

Cross-functional collaboration

Tools

eCTD submissions

Regulatory databases

Job description

Arrowhead Pharmaceuticals, Inc. is seeking a dynamic Regulatory Affairs professional to support multiple global regulatory projects, ensuring compliance with applicable requirements and developing regulatory plans.

You will report to the Director, Regulatory Affairs and work with cross‑functional teams to align strategies and submissions. The role focuses on IND/CTA/IMPD filings, health authority interactions, and global submissions, with opportunities to influence product development and