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Key Responsibilities:
- Lead integrated drug development strategies from preclinical through commercial stages.
- Provide expert guidance on clinical plans, regulatory submissions, and risk assessments.
- Support portfolio management, due diligence, and client engagements.
Requirements:
- Master's or higher in life sciences with 15–20+ years of global drug development experience.
- Proven expertise in clinical development strategy, regulatory affairs, and lifecycle management.
- Strong analytical, communication, and cross-functional leadership skills.
Benefits:
- Competitive salary with performance-based compensation and bonuses.
- Comprehensive health coverage, retirement plan, and paid time off.
- Flexible remote work, professional development, and global scientific engagement.
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