Remote Regulatory Affairs Manager – Biologics & Cell Therapy

Iovance Biotherapeutics, Inc.

United States

Remote

USD 125,000 - 180,000

Full time

14 days+

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Job summary

Scorpion Therapeutics seeks a Manager of Regulatory Affairs to lead global regulatory submissions for investigational and marketed biologics, with a focus on cell therapy. The role covers INDs, BLAs, amendments, and submission strategies, with emphasis on ICH compliance and cross-functional teamwork.

The position requires 8+ years in regulatory affairs, a BA/BS, and hands-on eCTD experience, with remote work to support global programs.

Qualifications

  • BA/BS required.
  • 8+ years in regulatory affairs or related drug/biologic development.
  • Experience with global electronic submissions (eCTD).
  • Regulatory agency interactions.
  • Regulatory strategy development.

Responsibilities

  • Manage INDs and BLAs.
  • Handle amendments and prepare documentation.
  • Maintain regulatory dossiers.
  • Coordinate cross-functionally.
  • Ensure compliance with international regulations (ICH).
  • Develop submission strategies.

Skills

Regulatory submissions
Regulatory strategy
Cross-functional collaboration
International regulatory compliance
Documentation management

Education

BA/BS
Advanced degree (preferred)

Tools

eCTD experience

Job description

Scorpion Therapeutics seeks a Manager of Regulatory Affairs to lead global regulatory submissions for investigational and marketed biologics, with a focus on cell therapy. The role covers INDs, BLAs, amendments, and submission strategies, with emphasis on ICH compliance and cross-functional teamwork.

The position requires 8+ years in regulatory affairs, a BA/BS, and hands-on eCTD experience, with remote work to support global programs.

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