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Key Responsibilities:
- Define and lead global regulatory strategy for clinical-stage radiopharmaceutical programs.
- Lead key regulatory submissions including INDs, CTAs, and DMFs.
- Serve as primary contact for regulatory agencies.
Qualifications & Education:
- Advanced degree in a scientific discipline preferred (JD, PhD, PharmD, MD).
- 15+ years of regulatory affairs experience in biotech or pharma.
- Proven track record of successful submissions (INDs, NDAs, BLAs, MAAs).
Personal Attributes:
- Foster a culture of excellence, collaboration, and continuous learning.
- Proactive, detail-oriented, and comfortable in a fast-paced biotech environment.
What We Offer:
- Unique chance to contribute to first-in-class cancer therapies.
- International, collaborative, and supportive work culture.
- Competitive compensation and benefits.
ARTBIO
ARTBIO discovers and develops a new class of Alpha Radioligand Therapies (ARTs) to redefine cancer care. It is a global biotech with offices in Boston, Basel, London, and Oslo, fostering a collaborative and supportive culture.