Senior Manager, Regulatory Affairs
Benefits
Unlimited PTO
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Job Responsibilities:
- Global Regulatory Lead for cutting-edge RPT programs.
- Clinical and nonclinical regulatory strategy for therapeutic and diagnostic products.
- Maintaining relationships with regulators.
Basic Qualifications:
- Bachelor’s degree or higher.
- 5+ years of hands-on regulatory experience.
- Experience with therapeutic and diagnostic radiopharmaceutical product development.
Skills:
- Excellent communication skills.
- Highly organized and able to multi-task.
- Strong communication and interpersonal skills.
RayzeBio
RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, develops transformative radiopharmaceutical therapies. They blend the spirit of an emergent biotech with the expertise and resources of a leading innovator in oncology, fostering a multidisciplinary team where ideas are valued.