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Director, Regulatory Affairs

Remote, USA Full-time Posted 2026-07-28

Bachelor's degree or higher; 10+ years regulatory affairs; FDA knowledge; NDA submissions; orphan drug/therapeutic area experience preferred; strong communication and planning.

Key Responsibilities

  • reputed company submissions
  • review documents
  • guide teams

Job Details

  • Category: Research and Development (R&D)
  • Seniority: Senior Level
  • Commitment: Full Time
  • Workplace: Remote — Princeton, New Jersey, reputed company
  • Languages: English

About F2G

Clinical-stage biopharmaceutical company developing novel antifungal therapies. — Industry: Research and Development

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