Vice President, Global Program Lead

About KalVista Pharmaceuticals, Inc.

KalVista Pharmaceuticals, Inc., is a global biopharmaceutical company dedicated to developing and delivering life-changing oral therapies for individuals affected by rare diseases with significant unmet needs. In the U.S., KalVista markets EKTERLY^®, the first and only oral on-demand treatment for hereditary angioedema (HAE). The Company has multiple regulatory applications under review in key global markets.

 For more information about KalVista, please visit www.kalvista.com and follow us on LinkedIn, X, Facebook and Instagram.

About Sebetralstat

Sebetralstat is a novel plasma kallikrein inhibitor approved in the United States and United Kingdom for the treatment of acute attacks of hereditary angioedema (HAE) in people 12 years of age and older. It is the first and only oral on-demand treatment for HAE. With ongoing studies exploring its use in children aged two to 11 and multiple regulatory applications under review in key global markets, sebetralstat has the potential to become the foundational therapy for HAE management worldwide.

 

About the Role:

We are seeking a dynamic leader with a strategic approach and strong communication skills to join us as Global Program Lead.  As a member of the senior leadership team, the person taking this role will be responsible for leading and ensuring execution of an integrated global program strategy including life-cycle management.  In this highly cross-functional role, you will lead global teams to deliver critical program milestones ensuring strategic alignment and compliance across all phases of the product lifecycle.

 

Responsibilities:

• End-to-End Program Leadership: Define program strategy, goals, multi-year plan, decision points, investments and areas of risk and associated mitigations and contingencies

• Stakeholder Engagement: Serve as an internal lead for the program, fostering broad engagement between functions and global and regional teams to ensure alignment and progress. Address scientific, medical, regulatory, commercial and operational needs to support the product's success
• Market Expansion: Support global rollout strategies, including regional launches and commercialization in new markets
• Commercial Support: Working closely with commercial, define strategies for competitor defense and strategic brand planning
• Lifecycle Management: Lead line extension activities through new developments such as indication expansion and new formulations to maximize the brand
• Project Planning & Cross-Functional Coordination: Act as the central point of contact for the program’s governance and communication; lead regular core team meetings and ensure integrated, cross-functional project plans are in place that span clinical, regulatory, commercial, medical, safety, supply chain, finance and corporate development. Ensure transparency of timelines, risks, and decisions to senior leadership
• Risk & Issue Management: Proactively identify and manage project risks and mitigation strategies, escalating critical issues appropriately
• Continuous Improvement: Contribute to development of best practices, tools, and frameworks with other project managers across the organization

Qualifications:

• Bachelor’s degree in Life Sciences, Pharmacy, or a related field (advanced degree preferred: PhD, PharmD, MD or MBA)
• 15+ years of biotech/pharmaceutical industry experience, with 10+ years of proven program leadership
• Proven experience managing global assets from late-stage development through commercial life cycle management, delivering success in a competitive market
• Demonstrated success working across matrixed, cross-functional teams, including Commercial, Medical Affairs, Regulatory, Manufacturing/Supply Chain and Corporate Development
• Excellent leadership, communication, and stakeholder management skills
• Proficiency with project management and collaboration tools (e.g., Smartsheet, MS Project, Teams)
• Strategic thinker with a holistic understanding of product lifecycle from development through to commercialization
• Comfortable managing ambiguity and adapting to shifting priorities
• Strong business acumen with a collaborative, solution-focused approach
• Culturally agile and able to lead across global teams and time zones
• Ability to travel internationally

Preferred Qualifications:

• PMP or equivalent certification
• Experience of working in small, medium sized enterprises (rather than “big Pharma”)
• Experience of small molecules
• Experience in rare disease
• Ability to travel internationally

 

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. 

Important Notice to Third-Party Recruiters & Staffing Agencies:

The current job openings advertised on this website are for the sole purpose of candidates to apply directly. Unsolicited and anonymous CVs submitted in any manner to KalVista employees, including to employee personal e-mail accounts, are considered to be the property of KalVista and will not qualify for a fee to be paid. Referral fees will only be payable where KalVista has agreed with an agency to work on a specific appointment, and then only in conjunction with a fully-executed contract for service.

If any Agency representative contacts a KalVista Hiring Manager or company employee, other than a member of the KalVista Talent Acquisition team, to solicit an appointment to engage on a job opening, that Agency will not be considered for that specific job opening or future opportunities with KalVista.

Thank you for your understanding and cooperation.