Korro Bio, Inc. · 9 hours ago
Senior Director/Vice President, Regulatory Affairs
Korro Bio, Inc. is a biopharmaceutical company focused on developing a new class of genetic medicines using its proprietary RNA editing platform. The Senior Director/Vice President of Regulatory Affairs will lead the development and execution of global regulatory strategies to support the clinical development and commercialization of the company’s pipeline, ensuring compliance and effective interactions with health authorities.
BiotechnologyHealth CarePharmaceutical
Responsibilities
Develop and implement global regulatory strategies aligned with corporate objectives for preclinical, clinical, and commercial programs
Serve as the primary regulatory contact for internal teams and health authorities (FDA, EMA, MHRA, PMDA, etc.)
Lead preparation and submission of INDs/CTAs, BLAs/NDAs/MAAs, and other key filings
Anticipate and mitigate regulatory risks; provide proactive guidance on evolving regulatory landscapes
Lead and execute in a lean organization while demonstrating hands-on, strong, cross-functional leadership across the organization to drive regulatory objectives and outcomes
Contribute to corporate strategy and participate in executive-level decision-making
Oversee all regulatory submissions, ensuring completeness, accuracy, and compliance with applicable regulations
Manage regulatory documentation systems and ensure inspection readiness
Lead interactions with external consultants, CROs, and regulatory agencies
Oversee development of labeling, promotional materials, and product claims
Partner closely with Clinical Development, CMC, Nonclinical, and project teams to align regulatory strategies with development plans
Serve as a trusted advisor to senior leadership on regulatory implications of corporate decisions
Foster a culture of accountability and innovation
Provide regulatory input to support business development and partnership activities
Mentor and develop peers to support both operational excellence and career growth
Qualification
Required
Advanced degree (PharmD, PhD, MD, or MS) in life sciences or related field
12+ years of progressive regulatory affairs experience in the biopharmaceutical industry, including leadership of regulatory strategy and submissions
Successful track record of interactions with FDA and global agencies, and experience leading major submissions (INDs, NDAs, BLAs, MAAs)
Deep understanding of global regulatory frameworks and guidelines
Proven ability to lead cross-functional initiatives and manage complex regulatory programs
Strong communication and interpersonal skills, with executive presence
Ability to thrive in a fast-paced, dynamic, and science-driven environment
Strategic thinker with operational excellence
High integrity and credibility with regulators and internal stakeholders
Collaborative leadership style with strong influencing skills
Entrepreneurial mindset and comfort operating in an emerging biotech setting
Preferred
Experience across multiple phases of development (preclinical through post-approval) strongly preferred
Benefits
Equity-based compensation
Medical
Dental
Vision
401(k) retirement plan
Life insurance
A dependent care flexible spending account
A Company-funded health savings account
Free parking
Company
Korro Bio, Inc.
Korro Bio was founded to turn extraordinary scientific insights into life-altering new treatments for patients.
Funding
Current Stage
Public CompanyTotal Funding
$277.5MKey Investors
Deep Track CapitalEventideWu Capital
2024-04-18Post Ipo Equity· $70M
2023-11-06IPO
2022-01-05Series B· $116M
Recent News
Genetic Engineering News
2025-11-19
Company data provided by crunchbase