Sr. Director / Exec. Director, Reg Affairs

Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical thoughtful use of AI to improve clarity, speed, and quality of work. What You'll Do #LI-TC1 As the Senior Director / Executive Director, Regulatory Affairs, you are a driven global regulatory leader with expertise in regulatory strategy development and execution. You excel in navigating global health authority interactions, leading cross-functional teams, and driving clinical and licensing submissions. Reporting to the QED Head of Regulatory Affairs, you will provide leadership in regulatory activities for assigned programs, including developing global regulatory strategies, leading submissions, and managing critical health authority interactions as well as leading regulatory staff. Responsibilities Provide leadership in creating and executing proactive regulatory strategies for product development, approval, and registration Apply knowledge of global quality/regulatory standards and guidelines to ensure requirements are met across programs Partner with internal senior leadership to align closely on cross-functional global regulatory plans and the company's short and long-term strategic objectives Take complete ownership of relevant regulatory submission deliverables Represent regulatory in senior management discussions and present strategies, recommendations, and risks accordingly Lead the specific Affiliate regulatory strategy team by managing, mentoring, and teaching capabilities Work at both high-level strategic and hands-on in leading an agile team Serve as key regulatory team member with responsibility for regulatory strategies and submissions lead asset Provide regulatory guidance and strategy for support of product development and registration strategies Ensure high-quality and timely regulatory submissions (IND/CTA/NDA/MAA/IDE/PMA, as applicable) in compliance with all applicable regulatory requirements, and in alignment with corporate goals Provide leadership and oversight of the preparation of all critical global regulatory submissions (from pre-IND to post-marketing) to the FDA, EMA, and other international health authorities Act as the primary liaison with regulatory authorities Direct and assist internal staff and regulatory consultants, as required, to ensure compliance of drug development activities with all U.S. and international requirements Analyze and communicate current regulatory guidance and regulations, as well as industry and regulatory agency best practices and trends, to keep company informed on any relevant changes in the regulatory landscape Support due diligence and partnering activities, as needed Perform all duties in keeping with the Company’s core values, policies and all applicable regulations Where You'll Work This a remote role and requires in-office collaboration quarterly in our San Francisco and Palo Alto. Who You Are Bachelor's degree in the scientific field is required; an advanced degree (MD, Ph.D., PharmD, MS) preferred A minimum of 15 years of relevant pharmaceutical/biotechnology regulatory affairs experience in ... (truncated, view full listing at source)