Director, Global Regulatory Affairs (Submission Project Management)

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence.

Requirements

• 10+ years (8+ with advanced degree) of regulatory affairs and/or project management experience
• Proven track record managing global submissions (NDA, BLA, MAA)
• Deep expertise in the integrated drug development process, ensuring seamless progression from discovery through commercialization

Benefits

• Comprehensive health coverage
• Flexible time off
• Paid holidays
• Year-end shutdown
• Monthly wellness stipend
• Generous 401(k) match
• Tuition reimbursement
• Commuter benefits
• Disability and life insurance
• Annual bonus opportunities
• Equity grants