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Supervisor, Reg Affairs US Legal
Partner Company
US
Regulatory Affairs
FDA Regulations
Quality Assurance
Key Responsibilities:
- Provide strategic medical leadership and oversight for clinical safety.
- Conduct hands-on review of SAEs and lead signal detection assessments.
Qualifications:
- MD or DO degree with 10+ years of pharmaceutical clinical development experience.
- Proven expertise in pharmacovigilance, safety signal detection, and global regulatory compliance.
Benefits:
- Fully remote role within the United States with an annual salary of $310,000-$350,000.
- Senior leadership opportunity to influence clinical safety strategy and development decisions.
Partner Company
The company is a clinical-stage biotechnology firm developing innovative therapies for pulmonary fibrosis and other serious respiratory diseases. It is a growing, lean organization with a focus on pharmacovigilance infrastructure and global clinical development.