Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japan-based company, our goal is to translate science into smiles by delivering therapies where no adequate treatments currently exist, working from drug discovery to product development and commercialization. In North America, we are headquartered in Princeton, NJ, with offices in California, North Carolina, and Mississauga, Ontario.
Summary of Job:
The Senior Director, Patient Advocacy, Engagement, and Policy is part of the NA Government Affairs organization. This role will lead development of patient-centric operating model across Kyowa Kirin North America disease franchises. The Senior Director, Patient Advocacy, Engagement and Policy is responsible for defining KKNA advocacy vision and strategy to engage patient communities across product life cycles, addressing commercial & global drug development activities. The Senior Director will partner with R&D and global business leaders to define and advance Kyowa Kirin’s model for patient engagement and advocacy from product development through post-approval and beyond.

Essential Functions:

• Lead, mentor, coach and train team members
• Act as both a player and a coach as being hands on directly involved in high impact work as well as leadership of the team
• Act as a leader in a global, cross-functional team in the creation and implementation of tools and training to support greater patient engagement in the global development process.
• Lead and manage patient and disease state advocacy efforts across franchise areas.
• Identify optimal strategic partners and opportunities for long-term collaborations that can help address patient needs
• Evaluate policy and regulatory landscape and opportunities to influence on behalf of patient needs
• Organize advisory boards and market research, as appropriate, to identify and understand patient needs and preferences; Use insights to continuously enhance clinical trial design, data generation, regulatory input, and market development efforts.
• Align and collaborate with Global Development leaders, Clinical Operations, Commercial Business leaders, and Regulatory and Medical Affairs teams on patient engagement activities.
• Manage/oversee patient advocacy portion of the annual corporate and brand planning process, collaborating with internal and relevant external stakeholders.
• Supervise and/or act as a project manager on assigned projects; Coordinate with vendors and teammates, as necessary, to execute contracts and SOWs, and to manage budgets and tactical execution.
• Engage and collaborate with alliance/JV partners, and global and cross-functional colleagues to fulfill these objectives.
• Provide ongoing internal updates to leadership and internal stakeholders.

Job Requirements:

EDUCATION

BA/BS required. LPN, MPH or MBA a plus

EXPERIENCE

At least 10 years of collective experience in advocacy, policy, or market development roles. Prior experience developing and managing successful Patient Advocacy collaborations. Knowledge of public policy and regulatory landscape. Demonstrates a thorough understanding of pharmaceutical development, the life sciences industry, and regulatory environments. Strategic thinker with excellent planning, writing, presentation, and interpersonal communication skills. Demonstrated experience building productive relationships with global, cross-functional stakeholders as well as advocacy organizations. Capable of driving projects from concept to execution autonomously; Adept at organizing work, analyzing, and solving problems, and coordinating contributions from multiple parties in order to achieve desired outcomes on time and on budget. Prior pharmaceutical or biotech experience or direct work for an advocacy organization is a plus.
Technical Skills
Proficient in MS Office Suite.

NON-TECHNICAL SKILLS

Demonstrated ability to organize, prioritize, meet deadlines, make decisions, and change course of action quickly. Strong interpersonal and communication skills. Strong work ethic is required. Detail oriented and excellent follow through. Has the ability to flex and deal with ambiguity in a dynamic, fast-paced, high growth environment. Has a passion for personal learning and development to be able to grow with the company. 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 10% domestic and international travel
The anticipated salary for this position will be $219,500 to $286,600. 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
• Discretionary Profit Share
• 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 kkus.talentacquisition.8h@kyowakirin.com. Controller’s data protection officer can be contacted at usprivacyoffice@kyowakirin.com. 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 usprivacyoffice@kyowakirin.com.

• Lead, mentor, coach and train team members
• Act as both a player and a coach as being hands on directly involved in high impact work as well as leadership of the team
• Act as a leader in a global, cross-functional team in the creation and implementation of tools and training to support greater patient engagement in the global development process.
• Lead and manage patient and disease state advocacy efforts across franchise areas.
• Identify optimal strategic partners and opportunities for long-term collaborations that can help address patient needs
• Evaluate policy and regulatory landscape and opportunities to influence on behalf of patient needs
• Organize advisory boards and market research, as appropriate, to identify and understand patient needs and preferences; Use insights to continuously enhance clinical trial design, data generation, regulatory input, and market development efforts.
• Align and collaborate with Global Development leaders, Clinical Operations, Commercial Business leaders, and Regulatory and Medical Affairs teams on patient engagement activities.
• Manage/oversee patient advocacy portion of the annual corporate and brand planning process, collaborating with internal and relevant external stakeholders.
• Supervise and/or act as a project manager on assigned projects; Coordinate with vendors and teammates, as necessary, to execute contracts and SOWs, and to manage budgets and tactical execution.
• Engage and collaborate with alliance/JV partners, and global and cross-functional colleagues to fulfill these objectives.
• Provide ongoing internal updates to leadership and internal stakeholders