Senior Director, Regulatory Operations

About Us Kardigan is a heart health company working to make cardiovascular disease preventable, curable and no longer the leading cause of death in the world. It is Kardigan’s mission to develop multiple targeted treatments in parallel that bring people with cardiovascular diseases to the cures they deserve. Led by Tassos Gianakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D., Kardigan’s co-founders have reunited after leading MyoKardia to discover and develop mavacamten, the first cardiac myosin inhibitor, resulting in an acquisition by Bristol Myers Squibb in 2020. We have a cutting-edge discovery and translational research platform, a pipeline of late-stage candidates, and an industry-leading team that is driven to improve the lives of patients. At Kardigan, we are motivated by our values which guide how we work, interact, and achieve our goals. Driven by patients and their families , we are deeply committed to improving the lives of patients and prioritizing their needs above all else. We believe in being authentic —leading with truth to bring out the best in others by creating an environment where every person knows they will be fully accepted. With an eagerness to learn , we encourage the highest levels of curiosity and are open to changing our minds. We are committed to winning as a team with urgency, excellence, and intention, and support each other no matter what role we play or where we sit. Lastly, we strive to enable the impossible because patients are counting on us. We are not afraid to take risks to unlock innovation and advance scientific discoveries. These values are the foundation of our work, empowering us to make a real difference, every day. Position Title: Senior Director, Regulatory Operations Department: Regulatory Reports To : SVP, Head of Regulatory Location: South San Francisco, CA (preferred) or Princeton, NJ – On site 4 days a week (Mon to Thurs) Job Overview Kardigan is seeking an experienced Senior Director, Regulatory Operations. Reporting directly to the SVP of Regulatory, the Senior Director will oversee global Regulatory Operations across Kardigan’s portfolio. This role is responsible for end-to-end management of global regulatory submissions, ensuring timely and compliant publishing, electronic submission and archival. The Senior Director will partner closely with Regulatory and cross-functional team members to deliver high quality, inspection ready submissions aligned with corporate objectives. This role will ensure or establish best practices for Regulatory Operations. Key Responsibilities Regulatory Submission Planning, Strategy & Execution Oversee all regulatory submission types (eg, IND, CTA, NDA, MAA, and amendments) across Kardigan’s portfolio. Manage planning, publishing, electronic submission, and archival of regulatory submissions. Establish clear lines of communication with stakeholders to align regulatory plans that maximize efficiency and quality of regulatory submissions. Regulatory Operations Leadership & Team Management Build, mentor, and manage a high-performing Regulatory Operations team, including contractors and vendors, to achieve overall corporate objectives. Manage external vendors, CROs, and consultants for performance and budget. Set clear goals and expectations, supporting continuous improvement and accountability. Support cross-functional employee on-boarding and training by providing technical support to stakeholders and project team members as needed. Support Regulatory budgeting and forecasting activities, including review of expenditures for activities related to vendor contracts. Systems, Tools & Process Optimization Maintain and enhance regulatory systems and tools (RIM, publishing, document management, templates and relevant style guides). Partner with IT/business teams on validation and upgrades. Develop and implement SOPs and standardized processes, drive process optimization. Compliance, Inspection Readiness & Governance Ensure operational compliance with global regulations and internal policies. Lead inspection readiness, training, and documentation oversight. Monitor regulatory changes and assess their impact. Qualifications and Preferred Skills Bachelor’s degree in a scientific, life sciences, or related field required. Advanced degree (MS, PhD, PharmD) preferred. 10+ years of relevant industry experience, with majority of experience in Regulatory Operations. Demonstrated experience leading global regulatory submissions across multiple regions. Experienced in building and leading teams and managing outsourced partners. Strong experience with eCTD publishing, regulatory systems (e.g., RIM), and regulatory document management. Experience driving regulatory operations transformation or system implementations. Experience supporting late stage development and regulatory inspections preferred. Deep understanding of global regulatory submission requirements and health authority expectations. Strategic thinker with strong execution, problem solving, and change management skills. Excellent communication, collaboration, and stakeholder management abilities. Strong organizational and project management skills with high attention to detail. Ability to operate effectively in fast paced, evolving environments while maintaining quality and compliance. Exact Compensation may vary based on skills, experience and location. Pay range $248,000 — $333,000 USD

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