Global Biologics Regulatory Strategy Lead

Scorpion Therapeutics

Gaithersburg (MD)

Hybrid

USD 180,000 - 300,000

Full time

14 days+
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Job summary

Scorpion Therapeutics seeks a Senior Director of Regulatory Affairs to oversee global regulatory strategies for biologics development, with a focus on late-stage filings. The role is based in Gaithersburg, MD or Radnor, PA, with potential for global interaction and oversight.

You will lead IND, BLA, and sBLA submissions, develop regulatory strategies, and mentor cross-functional teams while ensuring compliance with US and international regulations.

Qualifications

  • Advanced degree (MS, PharmD, PhD, or MD) with 8–12 years of experience (MS) or 10–15 years (BS).
  • Extensive knowledge of US and global regulatory environments.
  • Proven experience in preparing IND/CTA, BLA/NDA submissions, including at least one NME BLA/NDA.

Responsibilities

  • Lead IND, BLA, and sBLA submissions.
  • Develop regulatory scientific and tactical strategies.
  • Liaise with FDA, EMA, MHRA and health authorities.
  • Oversee regulatory documentation including CTDs, briefing documents, labeling.
  • Provide leadership within cross-functional teams and mentor direct reports.
  • Ensure compliance with global regulatory requirements.
  • Contribute to procedures for late-stage development and commercialization.
  • Manage health authority interactions and review clinical trial labeling and CMC submissions.

Skills

Regulatory submissions
Leadership
Cross-functional collaboration
Communication
Biologics

Education

Advanced degree (MS/PharmD/PhD/MD)

Job description

Scorpion Therapeutics seeks a Senior Director of Regulatory Affairs to oversee global regulatory strategies for biologics development, with a focus on late-stage filings. The role is based in Gaithersburg, MD or Radnor, PA, with potential for global interaction and oversight.

You will lead IND, BLA, and sBLA submissions, develop regulatory strategies, and mentor cross-functional teams while ensuring compliance with US and international regulations.

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