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An established industry player is seeking a Director of Medical Affairs to lead Canadian strategies in oncology and rare diseases. This pivotal role involves collaborating with cross-functional teams, managing stakeholder interactions, and ensuring compliance with regulatory standards. The ideal candidate will possess a strong background in medical affairs, excellent communication skills, and the ability to thrive in a fast-paced environment. Join a forward-thinking company dedicated to transforming science into innovative therapies and making a meaningful impact in patients' lives.
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 Director, Medical Affairs Canada leads, manages, and supports all aspects of Canadian Medical Affairs strategy and is accountable for the implementation of medical tactics for Kyowa Kirin Canada. This person serves as an integral member of internal cross-functional teams, the Canadian management team, and the Kyowa Kirin North America (KKNA) Medical Affairs Leadership team. This role is accountable for Medical Affairs interactions with internal / external stakeholders, including but not limited to Canadian Medical Affairs strategy, Evidence Generation, and dissemination including publications, Sponsored testing programs, promotional material review, and medical material review, Medical materials generation and review, Medical Information, Medical Education, Medical Training, Special Access Programs, and Compassionate Use Programs. This role will also support Canadian MSL activities.
Essential Functions :
Education
Advanced degree in Health Sciences (MD, PhD, PharmD) or closely related discipline.
Experience
This position requires a minimum of five (5) years of relevant industry experience, including Medical Affairs. Experience in Rare Disease is preferred. Proven track record, including overseeing product launches and lifecycle management. Deep understanding of pharmaceutical R&D, clinical and commercialization processes in Canada. Current knowledge of all relevant industry, legal, and regulatory compliance guidelines. Excellent written and spoken English. French proficiency is preferred. Excellent oral, written, and presentation skills and ability to effectively communicate with a diverse range of stakeholders. Strong analytical skills, attention to detail, and ability to manage / prioritize multiple projects from conception to completion in a fast-paced environment.Ability to work well in cross-functional teams (across geography and culture) with people with diverse skill sets and personalities. Team player, flexible and adaptable. Ability to build strong, trusted working relationships, both inside and outside the organization. Knowledge of, and experience supporting Canadian HTA reviews and reimbursement negotiations for new drugs and indications. Commitment to the highest ethical, legal, regulatory, and scientific standards. Eligibility to work in Canada.
Technical Skills
Outstanding leadership abilities include demonstrated capacity to lead, inspire and build collaborative relationships. In-depth understanding of drug development, legal and regulatory compliance guidelines. Excellent communication skills (written, verbal, listening, and presentation). Solid proficiency using Microsoft Office Suite including Word, Excel, and Power Point for documentation, analysis, and presentations.
Non-Technical Skills
Demonstrated ability to organize, prioritize, meet deadlines, make decisions, and change course of action quickly. Commitment to the highest ethical, legal, regulatory, and scientific standards in all aspects of work 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.
Travel
Requires up to 20% domestic and international travel.
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.
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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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