Kyowa Kirin is a global specialty pharmaceutical company backed by more than 70 years of breakthrough life science innovation, dedicated to discovering and advancing treatments for diseases in which unmet need is greatest. Based in Japan with worldwide operations, we work across the continuum from drug discovery to commercialization, guided by our commitment to patients and their families.

Our research teams, located in California and around the world, are focused on developing the next generation of antibody, cell, and gene therapies, with particular emphasis on bone and mineral disorders, hemato-oncology, and rare diseases. We accelerate development through collaborations with industry, academia, patients, and healthcare providers, and since 2018 we have introduced four new therapies serving patients with progressive illnesses often in need of new therapeutic alternatives.

Our culture is grounded in our values: Commitment to Life, Integrity, Innovation, and Teamwork/Wa, and brought to life through the Kabegoe Principles, which define the behaviors and actions that guide how we work together to deliver meaningful impact for patients.

We’re proud of the progress we’ve made and mindful of the countless individuals still waiting for their own breakthroughs. A commitment to making people smile unites our efforts. Learn more at www.kkna.kyowakirin.com.

Summary of Job:

The Global Medical Affairs Therapeutic Area Head, Rare Disease, provides strategic scientific and medical leadership for the Rare Disease portfolio within Kyowa Kirin. Reporting to the Global Head of Medical Affairs, the position is a member of the Global Medical Affairs Leadership Team and is accountable for the development and execution of global Medical Affairs strategies and plans across the therapeutic area.

This role is accountable for leading the development and delivery of the Rare Disease Global Medical Affairs Strategic Plans, including evidence generation, scientific communications, publications, external partnerships, and launch readiness, while ensuring alignment with business and franchise priorities. Success requires close collaboration across Franchise, Regional Medical, HEOR, Patient Advocacy, Market Access, Commercial, Legal and Compliance, and Regulatory Affairs, R&D functions to support integrated execution of Medical Affairs strategies.

Strategic medical input is provided to clinical development and regulatory strategies in Rare Disease, incorporating patient, physician, and payer perspectives and supporting health technology assessment (HTA) and payer strategies. The position also provides medical and scientific expertise to Business Development, Regional Medical, and Regional Business teams in the evaluation and prioritization of potential assets, including due diligence and portfolio decisions, and supports the successful execution of partnering activities.

Essential Functions:

Strategic Leadership and Medical Expertise

• Provide comprehensive subject matter expertise, scientific, medical and technical knowledge of products and disease area landscapes for marketed and development portfolio within Rare Disease Therapy Area.
• Significant contributor to Integrated Asset Plans and Integrated Evidence Generation Plans
• Develop and execute the Global Medical Affairs Strategy for the Rare Disease Therapy Area (TA) portfolio, in alignment with business and franchise priorities, and the Integrated Asset Plan
• Ensure consistency of medical affairs strategy and execution between regions (NA/EMEA/JAPAC), incorporating regional insights and supporting regional medical needs within the global medical strategy.
• Lead the development of medical communication platforms and scientific narratives for Rare Disease products across the lifecycle
• Partner with Global Development Organization to provide medical and strategic input into clinical development programs, including study design, protocol development and interpretation of results
• Provide medical and scientific input for the development of Life Cycle Management strategies
• Collaborate with the Franchise and commercial teams providing medical input into the Target Product Profile (TPP) of portfolio compounds and into Brand Plans
• Support payer/market access strategy with HEOR and Market Access colleagues.
• Conduct timely medical assessments for business development due diligence activities, as a medical and scientific expert, in partnership with the North American Medical Affairs head and North American business teams and global cross-functional teams
• Establish and chair regular global-regional medical affairs meetings and participate in Franchise and other cross-functional meetings
• Support the Global Research organization as requested with medical insights and expertise
• Participate in cross-functional leadership teams and governance committees
• Review and approve applicable medical, commercial, regulatory, quality and pharmacovigilance documents

Evidence Generation

• Develop and deliver global integrated evidence generation plans and evidence dissemination plans including specific needs for Phase 4/post-registration studies including HEOR and Real-World Evidence (claims databases, registries etc.).
• Oversee approval process and support for unsolicited investigator sponsored trial proposals
• Develop and implement post-marketing studies and/or registries, as needed in collaboration with HEOR/RWE
• Lead the development of publication strategies and medical communications plans
• Develop and implement pre-authorization Early Access Programs, as approved by enterprise governance bodies

External Engagement

• Establish and maintain strong relationships with key external experts, healthcare professionals, professional societies and patient advocacy groups
• Serve as a key medical expert and thought leader, representing Kyowa Kirin at scientific conferences, advisory boards and key stakeholder meetings
• Drive scientific exchange programs and medical education initiatives
• Collaborate with external research partners and academic institutions

Team Leadership and Development

• Build, mentor and lead a high-performing global-regional medical affairs team, in accordance with the principles of high-performing teams
• Ensure alignment in execution of medical affairs activities through Medical Directors, Medical Science Liaisons (MSLs), Medical Information, Medical Communications and HEOR teams within Rare Disease
• Ensure that medical personnel at global, regional and local levels are properly trained, equipped and aligned with consistent scientific and medical messages and tools
• Foster a culture of scientific excellence and continuous learning
• Manage budget and resources effectively
• Provide ethical and compliant leadership by example, embracing the Kyowa Kirin core values of integrity, innovation, teamwork/wa and commitment to life, and the Kyowa Kirin Kabegoe Principles

Governance and Compliance

• Ensure compliance with SOPs, ethical standards and regulatory requirements across all activities
• Collaborate with cross-functional stakeholders to maintain governance frameworks for rare disease products

Job Requirements:

Education

Medical degree (MD, DO, MBBS, or equivalent) required. Advanced training or specialization in Rare Disease, clinical medicine, or a relevant therapeutic area preferred.

Experience:

• Minimum 15 years of experience in the pharmaceutical, biotechnology, or related healthcare industry, including at least 10 years in Medical Affairs and progressive leadership responsibilities at the global or enterprise level.

• Deep medical and scientific expertise in Rare Diseases, with comprehensive knowledge of disease biology, genetics, diagnostics, clinical practice, and evolving treatment landscapes.

• Strong track record of shaping and executing global Medical Affairs strategies that enhance product value, differentiation, evidence generation, and lifecycle management across development and commercial stages.

• Significant experience across the drug development lifecycle, including clinical development, study design, protocol development, clinical data interpretation, regulatory strategy, and post-marketing evidence generation.

• Broad track record in medical and scientific due diligence, including evaluation of external assets, business development opportunities, partnerships, collaborations, and portfolio priorities.

• Leadership of global, cross-functional, and geographically dispersed teams, with the ability to align regional and global Medical Affairs strategies and drive consistent execution across markets.

• Well-established relationships with external scientific and medical stakeholders, including key opinion leaders, healthcare professionals, professional societies, patient advocacy organizations, and academic or research institutions.

Technical Skills:

• Ability to set strategic direction, make sound decisions in complex and ambiguous environments, and translate scientific and medical insights into clear strategic priorities and actions.
• Evaluates complex scientific, clinical, and medical information and translate insights into actionable recommendations for portfolio strategy, evidence generation, clinical development, and lifecycle planning.
• Critically assesses clinical, scientific, epidemiologic, health economics, and real-world evidence and synthesizes complex information to inform strategic decisions
• Applies knowledge of global drug development processes, regulatory environments, and applicable legal, compliance, ethical, and pharmacovigilance requirements to strategic and operational decision-making.
• Influences and aligns senior stakeholders across Medical Affairs, R&D, Regulatory, Market Access, HEOR, Commercial, Patient Advocacy, and other functions, including in situations where formal authority is limited.
• Connects medical and scientific priorities with business objectives, franchise strategy, asset value, and portfolio priorities while maintaining appropriate medical independence.
• Inspires, coaches, develops, and aligns diverse teams while fostering scientific excellence, accountability, collaboration, and continuous learning.
• Effectively communicates complex scientific and medical concepts clearly and persuasively through written, verbal, presentation, and public speaking channels.
• Proficient in MS Office Suite.

Non-Technical Skills

• Excellent organizational abilities, including prioritization, decision-making and problem-solving
• Strong work ethic
• Detail oriented and excellent follow through
• Ability to flex and deal with ambiguity in a dynamic, fast-paced, high growth environment and matrix organization
• Passion and curiosity for personal learning and development
• Cultural sensitivity and ability to develop consensus within a multinational organization

Physical Demands: Normal office environment with prolonged sitting and extensive computer work.

Working Conditions: Requires up to 50% domestic and international travel

The anticipated salary for this position will be $394,200 to $492,800. The actual salary offered for this role at commencement of employment may vary based on several factors including but not limited to relevant experience, skill set, qualifications, education (including applicable licenses and certifications, job-based knowledge, location, and other business and organizational needs.

The listed salary is just one component of the overall compensation package. At Kyowa Kirin North America we provide a comprehensive range of benefits including:

• 401K with company match
• Annual Bonus Program (Sales Bonus for Sales Jobs)
• Generous PTO and Holiday Schedule which includes Summer and Winter Shut-Downs, Sick Days and, Volunteer Days
• Healthcare Benefits (Medical, Dental, Prescription Drugs and Vision)
• HSA & FSA Programs
• Well-Being and Work/Life Programs
• Life & Disability Insurance
• Concierge Services
• Long Term Incentive Program (subject to job level and performance)
• Pet Insurance
• Tuition Assistance
• Employee Referral Awards

The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

KKNA and all of its employees have an obligation to act in accordance with the law and with integrity in all our operations and interactions

It is the policy of Kyowa Kirin North America, Inc. to provide equal employment opportunity to all qualified persons without regard to race, religion, creed, color, pregnancy, sex, age, national origin, disability, genetic trait or predisposition, veteran status, marital status, sexual orientation or affection preference or citizenship status or any other category protected by law.

When you apply to a job on this site, the personal data contained in your application will be collected and stored by Kyowa Kirin, Inc. (“Controller”), which is located at 510 Carnegie Center Dr. Princeton, NJ 08540 USA and can be contacted by emailing [email protected]. Controller’s data protection officer can be contacted at [email protected]. Your personal data will be processed for the purposes of managing Controller’s recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 6(1)(f) of General Data Protection Regulation (EU) 2016/679 (“GDPR”) as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment.

Your personal data will be shared with Greenhouse Software, Inc., a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controller’s behalf. Accordingly, if you are located outside of the United States, your personal data will be transferred to the United States once you submit it through this site. The transfer will be made using appropriate additional safeguards under the standard contractual clauses approved by regulators for transfers of personal data outside the European Union.

Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment. Under the GDPR, if you are located in the European Union, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have the right to data portability, and to lodge a complaint with an EU supervisory authority. If you have any questions about our use of your data, you may contact us by email at [email protected].

Recruitment & Staffing Agencies

Kyowa Kirin does not accept agency resumes unless contacted directly by internal Kyowa Kirin Talent Acquisition. Please do not forward resumes to Kyowa Kirin employees or any other company location; Kyowa Kirin is not responsible for any fees related to unsolicited resumes.

#LI-JC1