Head of Regulatory Affairs

Summary
The Head of Regulatory Affairs leads ARTBIO’s regulatory function for clinical-stage radiopharmaceutical programs, ensuring clear strategy, compliant execution, and effective engagement with health authorities. This is a key leadership position that requires a deep understanding of regulatory processes and a proven track record of successfully navigating regulatory landscapes in the biotech or pharmaceutical industry.

Responsibilities

• Define and lead global regulatory strategy for ARTBIO’s clinical-stage radiopharmaceutical programs.


• Lead key regulatory submissions, including INDs, CTAs, and DMFs.


• Lead FDA and global health authority interactions, including meeting preparation, briefing packages, responses, and follow-up actions.


• Ensure compliance with regulatory requirements throughout the drug development lifecycle, including clinical trials and manufacturing.


• Proactively identify potential regulatory risks and develop mitigation strategies.


• Identify regulatory risks, advise executive leadership on timelines and decision points.


• Partner with Clinical, CMC, Quality, Nonclinical, Clinical Development and Operations, regulatory consultants, and external publishing partners to support timely, high-quality submissions.


• Serve as the primary point of contact for regulatory agencies and build strong relationships with key regulatory authorities.


• Monitor regulatory policy changes and provide practical guidance to internal teams on requirements, risks, and opportunities.


• Build regulatory capability through team leadership, mentoring, training, and strong cross-functional collaboration.

• Advanced degree (JD, PhD, PharmD, MD or equivalent) in a scientific discipline is preferred.


• 15+ years of regulatory affairs experience in the biotech or pharmaceutical industries, with emphasis on drug development.


• Possess in-depth knowledge of global regulatory requirements and guidelines, including FDA, and EMA regulations and international regulatory frameworks.


• Proven track record of successful regulatory submissions, including INDs, NDAs, BLAs and MAAs.


• Experience leading regulatory affairs strategies for complex programs across multiple therapeutic areas.


• Strong understanding of drug development processes, CMC, quality, and clinical trial regulations.


• Demonstrated ability to navigate complex regulatory landscapes and anticipate and mitigate potential regulatory risks.


• Familiarity with radiopharmaceuticals is a plus.

• Foster a culture of excellence, collaboration, and continuous learning.


• Proactive, detail-oriented, and eager to learn.


• Comfortable working in a fast-paced biotech environment.


• Team player who thrives on collaboration and cross-functional flexibility.


• Commitment to safety and continuous improvement.

• A unique chance to contribute to first-in-class cancer therapies.


• Exposure to both radiochemistry and CMC development in a dynamic biotech setting.


• Hands-on training and professional development opportunities.


• An international, collaborative, and supportive work culture.


• Competitive compensation and benefits.

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