Sr. Director, Corporate Compliance

Posted Yesterday
Be an Early Applicant
Hiring Remotely in USA
Remote
265K-295K Annually
Senior level
Biotech
The Role
Lead development and execution of a risk-based enterprise compliance program supporting commercialization readiness. Build governance, policies, monitoring, third-party diligence, training, reporting, and investigations. Serve as strategic partner to executive leadership, manage cross-functional initiatives and compliance team growth, and establish metrics to evaluate program effectiveness.
Summary Generated by Built In

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.  

  

Title: Sr. Director, Corporate Compliance 
Reports to: Chief Legal and Compliance Officer 
Location: Emeryville, CA (Hybrid) or west coast remote 


The Sr. Director, Corporate Compliance is responsible for developing and leading the company's enterprise compliance program as the organization transitions from clinical to commercial stage. This role establishes the vision, strategy, governance, and operations of a scalable, risk-based compliance program that supports responsible business growth, commercial readiness, and a culture of ethics and integrity.  

As a strategic leader and player-coach, the Sr. Director, Corporate Compliance provides enterprise-wide compliance leadership while remaining actively engaged in building and executing the program. Serving as a key member of the Legal leadership team, this role partners with executive leaders and cross-functional stakeholders to integrate compliance into the corporate strategy and business operations, proactively manage regulatory and ethical risk, and build the foundation for a high-performing Compliance function as the organization grows and transition into commercial stage. 

Responsibilities

  • Serve as the program manager for Kyverna’s enterprise compliance buildout and commercialization-readiness initiatives, coordinating cross-functional workstreams, owners, milestones, dependencies, deliverables, status reporting, and escalation of material blockers and risks.
  • Develop and execute the enterprise compliance program strategy and roadmap, in partnership with and under the direction of the Chief Legal Officer, aligning program priorities with corporate objectives and commercial-readiness milestones.
  • Lead the day-to-day operations of the Compliance function, establishing scalable governance, policies, systems, and processes that support sustainable organizational growth. 
  • Build and continuously enhance a risk-based enterprise compliance program, including healthcare compliance, aligned with the seven elements of an effective compliance program described in the HHS Office of Inspector General’s General Compliance Program Guidance.
  • Serve as a strategic thought partner to the Chief Legal Officer and executive leadership team, influencing corporate strategy by proactively identifying compliance risks, regulatory trends, and opportunities that impact business decisions. 
  • Establish meaningful compliance metrics and reporting to evaluate program effectiveness, inform executive decision-making, and drive continuous improvement. 
  • Build the Compliance function over time, recommending organizational structure, talent, and capabilities to support the company's evolving business needs. 
  • Partner with Commercial, Medical Affairs, Clinical Development, Regulatory Affairs, Market Access, Human Resources, Finance, Privacy, Legal, and other business leaders to embed compliance into business operations. Work closely with Legal on privacy-related compliance processes and escalate privacy legal issues to the appropriate Legal lead.
  • Provide practical guidance on healthcare compliance risks related to commercialization, including interactions with healthcare professionals, promotional activities, patient support programs, grants, speaker programs, and transparency requirements. 
  • Establish risk-based third-party compliance diligence, onboarding, monitoring, and recertification processes, and partner with Legal and business teams on compliance requirements and escalation procedures for higher-risk consultants, vendors, distributors, service providers, and strategic partners.
  • Balance effective risk management with business enablement, supporting innovation while maintaining regulatory compliance. 
  • Lead the development and ongoing effectiveness of the company's compliance program by: 

  • Establishing policies, standards, and governance processes. 
  • Developing compliance education and communications that promote ethical decision-making and a culture of integrity. 
  • Conducting enterprise compliance risk assessments and implementing monitoring activities to evaluate program effectiveness. 
  • Establish and manage compliance reporting channels, case-intake processes, and investigation protocols; oversee investigations, corrective actions, remediation plans, and continuous improvement initiatives. 
  • Measuring program effectiveness through data, metrics, and periodic program assessments. 
  • Operate as a strategic leader while remaining actively involved in execution during the company's growth phase. 
  •  
  • Develop trusted relationships across the organization and influence decision-making through collaboration, credibility, and sound judgment. 
  • Manage external compliance advisors, consultants, and the compliance budget, as appropriate, while establishing internal capabilities. 

Qualifications

  • Bachelor's degree in Business, Life Sciences, Healthcare Administration, or a related field; advanced degree (JD, MBA, MPH, MS, or equivalent) preferred.  
  • 12+ years of progressive experience in pharmaceutical, biotechnology, medical device, or healthcare compliance, including experience supporting commercial organizations.  
  • Demonstrated success building, standing up, or significantly enhancing enterprise compliance programs within a growing clinical-stage to commercial-stage biotechnology organization.  
  • Strong knowledge of healthcare compliance laws and regulations, including FDA promotional requirements, Anti-Kickback Statute, False Claims Act, Sunshine Act/Open Payments, PhRMA Code, HIPAA, and other applicable regulatory requirements.  
  • Proven ability to influence stakeholders while driving strategic compliance initiatives across the organization.  
  • Exceptional program and project management skills with demonstrated success leading complex, cross-functional initiatives involving multiple stakeholders, competing priorities, and evolving business requirements.  
  • Experience developing and executing multi-year compliance roadmaps, implementation plans, governance structures, and organizational change initiatives to support commercial readiness and business growth.  
  • Demonstrated ability to prioritize, manage, and execute multiple strategic initiatives simultaneously while meeting aggressive timelines and delivering measurable business outcomes.  
  • Experience establishing project governance, defining milestones, tracking deliverables, identifying risks and dependencies, and providing executive-level status reporting and communications.  
  • Strong organizational and operational leadership skills with the ability to translate strategic objectives into executable plans, allocate resources effectively, and drive accountability across cross-functional teams. 

The National salary range for this position is $265K to $285K USD annually. The San Francisco bay area salary range for this position is $275K-$295K This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on various factors, including without limitation individual education, experience, tenure, skills and abilities, as well as internal equity and alignment with market data.  This position is also eligible for bonus, benefits, and participation in Company’s stock plan.    

Skills Required

  • Bachelor's degree in Business, Life Sciences, Healthcare Administration, or related field
  • Advanced degree (JD, MBA, MPH, MS, or equivalent)
  • 12+ years progressive experience in pharmaceutical, biotechnology, medical device, or healthcare compliance, including supporting commercial organizations
  • Demonstrated success building, standing up, or significantly enhancing enterprise compliance programs in clinical-stage to commercial-stage biotech organizations
  • Strong knowledge of healthcare compliance laws and regulations (FDA promotional requirements, Anti-Kickback Statute, False Claims Act, Sunshine Act/Open Payments, PhRMA Code, HIPAA)
  • Experience building risk-based compliance programs aligned to HHS OIG's seven elements of an effective compliance program
  • Proven ability to influence stakeholders and drive strategic compliance initiatives across the organization
  • Exceptional program and project management skills leading complex, cross-functional initiatives
  • Experience developing and executing multi-year compliance roadmaps, governance structures, and organizational change initiatives for commercial readiness
  • Experience establishing project governance, defining milestones, tracking deliverables, identifying risks/dependencies, and providing executive-level reporting
  • Experience establishing third-party compliance diligence, onboarding, monitoring, and recertification processes
  • Experience managing compliance reporting channels, investigations, corrective actions, remediation plans, and continuous improvement initiatives
  • Strong organizational and operational leadership skills; ability to translate strategy into executable plans and drive accountability
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The Company
HQ: Emeryville, CA
55 Employees
Year Founded: 2018

What We Do

Kyverna is a cell therapy company engineering and developing a new class of curative living medicines for inflammatory and autoimmune diseases. Using its SmarTcell™ approach which includes synReg-T cell and synNotch CAR-T technology platforms, Kyverna reprograms T cells to target and selectively suppress or eliminate autoreactive immune cells. The company’s goal is to develop therapies that are selective, potent and durable to tame autoimmunity. We build interdisciplinary teams that bring a broad range of experiences and scientific expertise together to develop medicines that will free patients from the siege of autoimmune diseases and bring curiosity for exploring and creating the unknown. Our commitment to our employees is to foster an open, supportive, and inclusive environment where we create opportunities for individuals to learn and grow to their full potential at every level. synNotch is a trademark of Gilead/Kite.

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