Director
US$195,000 – US$330,000 / yr base salary
Posted 25 Jun 2026
Advertised as “Director or Senior Director, Regulatory Affairs”
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 8–12 yrs
- Management level
- People management
| Base salary | US$195,000 – US$330,000 / yr |
|---|
Field of studyscientific discipline
Study levelBachelor's
Study levelMaster's or higher
Who we are:
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn.
How we work:
- PIONEER: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.
- COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.
- BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.
How you’ll make an impact:
- Act as the global regulatory strategy lead for Kymera’s IRF5 degrader program, developing and driving the overall program regulatory strategy across multiple immunology and inflammation (I/I) indications.
- Ensure global regulatory strategies are effectively and efficiently implemented and maintained in line with evolving regulatory and business needs.
- Lead program teams through major regulatory filings and interactions, including INDs, CTAs/IMPDs, briefing packages, and health authority meetings.
- Serve as the primary regulatory partner on the IRF5 program team, working closely with Clinical, CMC, Nonclinical, Quality, and Commercial colleagues.
- Provide sound, science-based, solution-oriented regulatory guidance and advice to cross-functional program teams through strategic and flexible application of experience and regulatory knowledge.
- Clearly communicate regulatory risks, opportunities, and recommendations to program teams and senior leadership.