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Scientific Director, AML Medical Strategy & Communications

Princeton, New Jersey

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 Scientific Director, AML Medical Strategy and Communications will serve as a key leader within the North America Medical Affairs team in working with our alliance partner to help develop and shape medical strategy for a novel product(s) in AML and contribute to strategy across KKNA Oncology and the Oncology collaborative scientific and communications platform. Working closely with the Sr. Director – Oncology, this role will be responsible for shaping strategic direction, driving strategic projects, determining educational needs, and providing operational leadership for several areas. The Scientific Director is also a key member of internal cross-functional teams, and NAMAC (North American Medical Affairs Committee). This individual will serve as the central contact with internal/external stakeholders with respect to certain projects key external expert (KEE) planning, congress planning, and medical operations.

Essential Functions:

Focus on Strategy with internal/external stakeholders:

  • With alliance partner company, serve as KKNA Medical AML Medical lead and contribute to medical strategic plan as well as provide input to the Oncology Integrated Evidence Plan to guide purposeful data generation
  • Partner with the Oncology Sr. Director of Medical Affairs and contribute to the development of Medical Affairs strategy for commercialized product
  • Serve as lead AML Medical reviewer in promotional review process and ensure materials are scientifically accurate, current, and properly substantiated and referenced
  • Serve as Investigator-sponsored studies (IIS) lead to evaluate new proposals and provide oversight of existing IIS across Oncology
  • Provide medical strategic input during Franchise or Joint Collaborative Team Meetings
  • Represent KKNA at major scientific conferences and advisory boards to communicate medical insights and establish thought leadership in Oncology
  • Build and maintain relationship with KEEs, healthcare systems, and advocacy organization
  • Provide medical guidance and training to the cross-functional Oncology team and share relevant insights to contribute to strategy as well as support Medical Value Outcomes Liaisons, KKNA Medical Science Liaisons and relevant field teams
  • Contribute to key decision-making as a member of the NAMAC (North American Medical Affairs Committee) team

Focus on teamwork and cross-collaboration:

  • Align with and support other scientific/medical operational activities such as advisory board planning and execution, Medical Information tactics and MSL Training.

Other:

  • Ensure adherence to all applicable SOPs, policies, processes, and compliance guidelines.
  • Oversee vendor-related activities (selection, contracting, onboarding, day-to-day operation, performance evaluation, and improvement).
  • Additional projects and assignments as needed

Job Requirements:

Education

Advanced degree in Health Sciences or related field (MD, Ph.D., DNP, PharmD).

 

Experience

7 to 10 years of industry experience in Medical Strategy at pharmaceutical companies or at consulting agencies in the same respective area. Past record of success in determining medical affairs therapeutic area strategy. Direct experience with medical strategic planning and working with alliance partners are preferred. Deep understanding of pharmaceutical R&D and commercialization processes. Good knowledge of principles and practices of pharmaceutical clinical studies (including design, conduct, analysis, and reporting). Familiarity with Good Publication Practice, ICMJE guidelines, and other applicable industry guidelines.

 

Technical Skills

Proficient in MS Office Suite.

CMPP (Certified Medical Publication Professional) credentials are recommended.

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 30% domestic and international travel

 

The anticipated salary for this position will be $185,800 to $242,600.  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 matching
  • Discretionary Profit Sharing
  • 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
  • Long-Term Incentives
  • Life & Disability Insurance
  • Concierge Service
  • 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.

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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.

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