Job Summary
A company is looking for a Director of Global Regulatory Affairs - Neurosciences.
Key Responsibilities
- Lead the development and implementation of global regulatory strategies aligned with product team objectives
- Monitor global regulatory requirements and provide training and intelligence to ensure compliance and risk mitigation
- Serve as a strategic advisor on regulatory matters, representing the company in interactions with health authorities
Required Qualifications, Training, and Education
- Experience in regulatory affairs or related areas in pharmaceutical drug development
- Experience managing regulatory aspects of IND and global clinical trial activities
- Experience in CNS/sleep therapeutic area preferred
- PharmD, Bachelor's, Master's, or advanced degree in a scientific discipline
- Proven track record of collaboration with regulatory agencies, including the FDA
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