Senior Director, Regulatory Affairs

Evommune, Inc. is a private clinical-stage biotechnology company dedicated to revolutionizing the treatment of immune-mediated inflammatory diseases. Founded in 2020 by a leading team of R&D experts and biotech innovators, Evommune is headquartered in Palo Alto, California, with additional offices in New York, NY. Through groundbreaking science, we are committed to discovering, developing, and delivering therapies that not only address symptoms but also halt disease progression. Our pipeline focuses on advancing novel treatment options for underserved patient populations, targeting diseases at their root with best-in-class agents for safety and efficacy. For more information, visit www.Evommune.com.

Before we dive into the specifics of the role, it's important to highlight the core values that are integral to being a member of the Evommune team. Our values are not just words; they shape our culture, guide our decision-making, and define what it means to be part of our team.

Our core values

• Together We Win : We champion teamwork, celebrating every achievement as a shared success.
• Guided by Insight : We make data-driven decisions, using our collective experience to shape the future of our business.
• Every Day Matters : We act with urgency to bring transformative therapies to patients by being nimble, decisive, and effective.
• Driven By Excellence : We set a high bar and hold ourselves accountable to deliver exceptional results in everything we do.
• Empowered To Act : We invest in our team and value transparency, fostering trust and a sense of ownership.

We seek individuals who resonate with these principles, as they are essential for thriving in our collaborative, innovative, and dynamic work environment.

About the role

Evommune is seeking a highly motivated and experienced Senior Director of Regulatory Affairs to lead global regulatory strategy and operations across our development pipeline. This individual will be responsible for developing and executing regulatory strategies, overseeing submission activities (INDs, CTAs, NDAs / BLAs / MAAs), and partnering with internal stakeholders and external agencies to advance programs through clinical development and regulatory review.

This role requires deep regulatory expertise, scientific acumen, and strong cross-functional leadership in a fast-paced biotech environment.

This hybrid position is currently expected to be in our Palo Alto office 2 days a week with the option of working remotely 3 days a week.

What you'll do

Qualifications

Compensation

The salary range for this position is $250,000 - $275,000 and the position may be eligible for performance-based bonuses and / or equity-linked compensation. Salary ranges are determined by role, level and location and additional factors, including job-related skills, experience, and relevant education or training. We offer Company‑sponsored benefits, which include comprehensive health, dental and vision plans, and pet insurance. In addition, we provide a 401(k) plan, ample time off programs, paid parental leave, life insurance, disability insurance and an employee referral bonus program.

Evommune is proud to be an equal opportunity employer and will consider all qualified applicants for employment.

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