Key Responsibilities: - Single point of accountability for driving REM-422 program strategy and execution excellence. - Integrate clinical, regulatory, CMC, translational, medical affairs, and commercial functions into a coherent strategy. - Represent REM-422 at the Executive Leadership Team (ELT) and Board; develop and present program updates and go/no-go recommendations with clarity and rigor. - Manage the critical path, scenario plans, and risk registry with a bias toward proactive resolution. - Drive lifecycle considerations into the development strategy. - Partner with Regulatory Affairs to develop and execute a global regulatory strategy, including FDA, EMA, and other priority health authority engagement; oversee key submissions (IND amendments, briefing documents, NDA/BLA/MAA). - Actively

Key Responsibilities: - Single point of accountability for driving REM-422 program strategy and execution excellence. - Integrate clinical, regulatory, CMC, translational, medical affairs, and commercial functions into a coherent strategy. - Represent REM-422 at the Executive Leadership Team (ELT) and Board; develop and present program updates and go/no-go recommendations with clarity and rigor. - Manage the critical path, scenario plans, and risk registry with a bias toward proactive resolution. - Drive lifecycle considerations into the development strategy. - Partner with Regulatory Affairs to develop and execute a global regulatory strategy, including FDA, EMA, and other priority health authority engagement; oversee key submissions (IND amendments, briefing documents, NDA/BLA/MAA). - Actively