Remote Director, Regulatory Affairs

Summary

Join Syndax Pharmaceuticals as a Director, Regulatory Affairs to lead the development and implementation of a consolidated regulatory strategy for assigned products through all development phases.

Requirements

• Bachelor’s degree in scientific discipline; advanced scientific degree preferred
• Regulatory Affairs Certification highly desirable
• 10+ years pharmaceutical industry experience, including 7+ years in Regulatory Affairs leadership roles; Global experience desired
• Experience in multiple phases of development in various therapeutic areas
• Demonstrated experience in preparing FDA submissions
• Knowledge of the drug development process and global submission process
• Knowledge of global regulatory guidance as they relate to the overall global regulatory strategy

Responsibilities

• Develop and implement global regulatory strategy for assigned projects, along with Regional Regulatory Affairs representatives and Regulatory CMC
• Represent Syndax and communicate on all regulatory issues involving the FDA and other regulatory health authorities for all products and businesses
• Lead global and/or regional regulatory team on assigned projects
• Provides Leadership to Regulatory department. Responsible for training, development of the current regulatory team, and selection and hiring of new team members
• Develop and execute US regulatory strategy and contingencies for assigned projects
• Serve as the primary interface for FDA on assigned projects
• Responsible for the review and approval of Standard Operating Procedures (SOP) relating to preparation, submission and reporting information to regulatory authorities. Prepare, plan and implement new processes and policies to improve efficiency of the Company
• Communicate project regulatory strategies and plans to management, cross functional teams and any partners/collaborators to establish alignment
• Contribute to the development of competitive regulatory strategies that expedite development, maximize the probability of success, and mitigate risk
• Lead the preparation of submissions, which may include INDs, Briefing Documents, Orphan Drug Applications, and Marketing Applications, etc. Work with functional groups to define contributions to submissions. Lead regulatory submission teams for assigned projects
• Prepare company team for FDA and other health agency meetings, as required
• Serve as the primary interface with Regulatory CROs for coordination and preparation of submissions
• Maintain knowledge of global competitive landscape, regulatory environment, regulations and guidance