Angitia
Director, Global Regulatory Affairs
$180K–$230K
Remote with up to 20% domestic travel +1 · Remote · Director · Full-time · Posted Oct 5, 2026
- Location
- Remote with up to 20% domestic travel
Los Angeles, California, United States - Experience
- 10+ years of pharmaceutical or biotechnology experience, including at least 8 years in Regulatory Affairs strategy.
- Education
- Bachelor's degree in Life Sciences or related discipline; advanced degree preferred (PharmD, MS, PhD, MBA, or equivalent).
About the job
Leads global regulatory strategy and execution for development programs from early development through registration and lifecycle management.
What you'll do
- Lead regulatory strategy and represent Regulatory Affairs on cross-functional and governance teams.
- Guide health authority interactions and oversee major regulatory submissions, including INDs, CTAs, amendments, and marketing applications.
- Advise teams and senior management on regulatory risks, development plans, and evolving requirements; mentor regulatory professionals.
What they ask for
- 10+ years of pharmaceutical or biotechnology experience, including at least 8 years in Regulatory Affairs strategy.
- Significant experience supporting global development programs through registration and lifecycle management.
- Strong knowledge of regulatory requirements and frameworks in the US, EU, and Japan.
- Experience leading health authority interactions, developing major regulatory submissions, and regulatory strategies.
Nice to have
- Advanced degree (PharmD, MS, PhD, MBA, or equivalent).
- Experience in rare disease, orphan drug development, or other specialized development pathways.
Pay
$180k - $230k (base salary; currency not stated)
Model-written summary · the original posting is authoritative