About BridgeBio
Bridging science and hope for genetic diseases
Key Highlights
- Public company (NASDAQ: BBIO) with strong market presence
- Over 15 drug development programs targeting rare genetic diseases
- $1.5B+ raised from top investors like OrbiMed
- Headquartered in Palo Alto, California
BridgeBio (NASDAQ: BBIO) is a biopharmaceutical company headquartered in Palo Alto, California, focused on developing innovative medicines for genetic diseases. With a pipeline of over 15 programs, BridgeBio aims to address unmet medical needs for rare genetic conditions, leveraging advancements in ...
🎁 Benefits
BridgeBio offers competitive salaries, equity options, comprehensive health benefits, and generous PTO policies. Employees also enjoy a flexible work ...
🌟 Culture
BridgeBio fosters a culture of innovation and collaboration, emphasizing the importance of scientific rigor and entrepreneurial spirit. The company va...
Overview
BridgeBio is hiring a Senior Director of Regulatory Affairs to lead global regulatory strategy and execution. You'll navigate health authority interactions and manage submissions for groundbreaking biopharma advancements. This role requires extensive experience in regulatory affairs.
Job Description
Who you are
You are a seasoned regulatory affairs professional with a proven track record in developing and executing regulatory strategies for biopharmaceutical products. With over 10 years of experience in the industry, you have successfully navigated complex interactions with global health authorities and led cross-functional teams to achieve regulatory milestones. Your expertise in clinical and licensing submissions sets you apart as a leader in the field.
You thrive in dynamic environments where innovation is key, and you are passionate about advancing therapies for patients with unmet medical needs. Your ability to think strategically while managing the details of regulatory processes ensures that your teams are well-prepared for every submission and interaction. You are known for your strong leadership skills, fostering collaboration among diverse teams to drive successful outcomes.
What you'll do
As the Senior Director of Regulatory Affairs, you will be responsible for creating and executing proactive regulatory strategies for assigned programs. You will lead the development of regulatory submissions and manage critical interactions with health authorities, ensuring compliance with all regulatory requirements. Your role will involve mentoring and guiding regulatory staff, fostering a culture of excellence and continuous improvement within the team.
You will collaborate closely with cross-functional teams, including clinical, manufacturing, and commercial, to align regulatory strategies with business objectives. Your insights will be crucial in shaping the regulatory landscape for our innovative therapies, and you will play a key role in defining the future of biopharma at BridgeBio.
What we offer
At BridgeBio, we offer a competitive salary range of $270,000 to $320,000 USD, along with a comprehensive benefits package that supports your health and well-being. You will have the opportunity to work alongside some of the most respected minds in the industry, contributing to groundbreaking advancements in rare disease therapies. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse perspectives and backgrounds.
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