Senior Regulatory Scientist
A company is looking for a Senior Regulatory Scientist to support a Solid Oral Phase II & III program.
Key Responsibilities
• Execute regional clinical trial submission strategies for US, EU, and China
• Prepare, review, and coordinate regulatory documents for clinical trial applications
• reputed company cross-functional collaboration to ensure compliant submission packages
Required Qualifications
• 7-10+ years of regulatory affairs experience in clinical-stage drug development
• Solid experience with solid oral dosage programs strongly preferred
• Proven ability to work independently and deliver to aggressive timelines
• Strong understanding of Phase II & III regulatory requirements
• Bachelor's or advanced degree in a life science or reputed company field (MS/PhD preferred)
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