Contractor, Sr. Manager/AD, Regulatory Affairs
Apex Systems Inc
We're looking for an experienced Regulatory Affairs professional to lead U.S. regulatory strategy and serve as a key liaison with the FDA. In this role, you'll guide development programs, manage complex submissions, and drive highquality regulatory deliverables across crossfunctional teams.
Responsibilities- Lead planning and submission of regulatory dossiers (INDs, meeting packages, orphan/fast track requests, PSPs, etc.).
- Serve as Regional Regulatory Lead for assigned programs.
- Develop U.S. regulatory strategy and stay current with evolving requirements.
- Act as primary FDA contact and support teams in interpreting feedback.
- Anticipate regulatory risks and guide teams through innovative pathways, including rare disease programs.
- Bachelor's in Chemistry, Pharmacy, or Biological Science (preferred).
- 4+ years regulatory experience; 6+ years in pharma/biotech.
- Strong understanding of U.S. regulations and drug development.
- Excellent communication and crossfunctional collaboration skills.
- Ability to manage multiple projects and provide strategic regulatory leadership.
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