Associate Director, Regulatory Affairs

RayzeBio

San Diego, CA, United States
Base: $173,217 - $209,899 (remote us) or $190,539 ...
Fully remote
7+ years regulatory experience in oncology
Experience with therapeutic and diagnostic radiopharmaceuticals
Familiarity with radioisotopes like 68ga, 177lu, 225ac
RayzeBio is developing transformative radiopharmaceutical therapies to improve survival for people with cancer by harnessing targeted radioisotopes

Job Summary

  • RayzeBio is developing transformative radiopharmaceutical therapies to improve survival for people with cancer by harnessing targeted radioisotopes.
  • The Global Regulatory Lead will oversee regulatory functions, manage direct reports, and lead the preparation of critical regulatory filings and authority interactions.
  • Employees receive comprehensive benefits including health coverage, financial protection plans, flexible time off, and eligibility for stock opportunities.

Matching Summary

RayzeBio is developing transformative radiopharmaceutical therapies to improve survival for people with cancer by harnessing targeted radioisotopes.

Salary

Base: $173,217 - $209,899 (Remote US) or $190,539 - $230,888 (San Diego); Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • 7+ years regulatory experience in oncology
  • Experience with therapeutic and diagnostic radiopharmaceuticals
  • Familiarity with radioisotopes like 68Ga, 177Lu, 225Ac
  • Expertise in IND, CTA/IMPD, and marketing application submissions
  • Proven leadership in cross-functional regulatory teams

Nice-to-have

  • Ability to anticipate changes in standard of care
  • Strong written and verbal communication skills
  • Meticulous attention to detail and precision
  • Flexibility to adapt in a dynamic environment
  • Proficiency in MS Office and video conferencing tools

Key Requirements

  • Bachelor's degree or higher
  • 7 or more years of hands-on regulatory experience
  • Experience with nonclinical and clinical regulatory strategy in oncology

Work Rights

Not specified

Tailored Resume

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