Senior Medical Science Liaison – Ontario

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 make people smile by delivering breakthroughs 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, Massachusetts, and Ontario

Ontario Territory – Field Based Candidates may reside anywhere within the province of Ontario, with proximity to a major airport required.

Summary of Job

The Medical Science Liaison (MSL) is a field-based member of the Medical Affairs organization responsible for serving as a scientific and clinical expert for the company's therapeutic area(s) and products. The MSL establishes and maintains trusted scientific relationships with healthcare professionals (HCPs), key opinion leaders (KOLs), researchers, and other external stakeholders to facilitate the exchange of accurate, balanced, and evidence-based scientific information.

The role supports Medical Affairs objectives by providing scientific and clinical expertise, gathering actionable medical insights, and contributing to evidence generation and medical strategy while ensuring all activities are conducted in compliance with applicable regulations, industry standards, and company policies.

Essential Functions

Establish, develop, and maintain strategic scientific relationships with national, regional, and local key opinion leaders (KOLs), healthcare professionals (HCPs), investigators, and other external stakeholders.

Serve as a trusted scientific expert by engaging in compliant, peer-to-peer scientific exchange and providing accurate, balanced, and evidence-based medical and clinical information regarding Kyowa Kirin products, disease states, and emerging clinical data, including responses to unsolicited medical information requests.

Gather, analyze, and communicate actionable medical insights, unmet medical needs, and competitive intelligence from field interactions to inform Medical Affairs strategy, evidence generation, and cross-functional decision-making.

Function as the regional scientific expert by identifying external stakeholder needs and connecting them with appropriate Medical Affairs resources, initiatives, and scientific collaborations.

Support the planning and execution of Medical Affairs objectives through scientific engagement at national, regional, and local medical congresses, advisory boards, investigator meetings, and other scientific forums.

Establish and maintain collaborative relationships with clinical investigators and support investigator-initiated studies (IIS) and company-sponsored clinical research in partnership with Clinical Operations, in accordance with company policies and regulatory requirements.

Develop and deliver scientific presentations, educational programs, and clinical resources for healthcare professionals and other appropriate stakeholders.

Deliver scientific education and training to internal cross-functional partners on disease states, therapeutic landscapes, clinical data, and Kyowa Kirin products.

Build and maintain effective cross-functional partnerships across Medical Affairs, Clinical Development, Commercial, Market Access, Regulatory Affairs, and other internal functions while maintaining appropriate boundaries between scientific and commercial activities.

Communicate important product safety information in accordance with Medical Affairs, Research & Development, pharmacovigilance, and applicable regulatory requirements.

Maintain current scientific knowledge through continuous review of clinical literature, treatment guidelines, and emerging data within assigned therapeutic area(s).

Disseminate product safety information to healthcare professionals in accordance with Medical Affairs, Research & Development, regulatory requirements, and company policies.

Participate in cross-functional projects, Medical Affairs initiatives, and strategic planning activities, serving as a scientific resource to internal stakeholders.

Mentor and support the development of fellow MSLs by sharing scientific expertise, field insights, and best practices, as appropriate.

Perform all responsibilities in compliance with applicable laws, regulations, industry codes, company policies, and the highest standards of scientific integrity and ethical conduct

Education

Advanced clinical or scientific degree or healthcare professional credential required (e.g., MD, PhD, PharmD, NP, MSc, or equivalent).

Doctoral degree (MD, PhD, or PharmD) preferred.

Experience

Minimum of four (4) years of experience as a Medical Science Liaison (MSL), field-based medical professional, or in a related clinical, scientific, or Medical Affairs role preferred.

Background in the Rare Disease therapeutic area or related disease state (e.g., Metabolic Diseases, Oncology, or Hematology) preferred.

Demonstrated ability to engage healthcare professionals (HCPs), key opinion leaders (KOLs), investigators, and other external stakeholders through compliant scientific exchange.

Ability to interpret and communicate clinical and scientific data effectively to diverse audiences.

Familiarity with clinical research activities, including investigator-initiated studies (IIS) and/or company-sponsored clinical trials, preferred.

Involvement in scientific congresses, advisory boards, investigator meetings, or other medical education activities preferred.

Track record of effectively managing field-based responsibilities, prioritizing activities, and operating independently in alignment with Medical Affairs objectives.

Technical Skills

Understanding of assigned disease states, therapeutic landscapes, treatment guidelines, and current standards of care.

Familiarity with clinical research methodology, evidence generation strategies, and interpretation of clinical trial data.

Working knowledge of Health Canada regulations, Good Clinical Practice (GCP), pharmacovigilance requirements, and applicable industry standards.

Proficiency in evaluating medical literature, synthesizing scientific information, and translating complex data into meaningful insights for healthcare professionals and internal stakeholders.

Skilled in delivering scientifically accurate, balanced, and compliant presentations to external and internal audiences.

Experience utilizing Medical Affairs systems, customer relationship management (CRM) platforms, and proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).

Demonstrated capability to analyze medical insights, identify trends, and support data-driven decision-making within Medical Affairs.

Capacity to manage multiple priorities, organize field-based activities, and operate effectively in a dynamic, cross-functional environment.

Outstanding interpersonal skills, including the ability to build strong working relationships and effectively manage conflict.

Excellent written, verbal, listening, and presentation skills.

Fluent in English – written and verbal. Bilingual English/French preferred

Non-Technical Skills

Ability to thrive in a fast-paced environment while managing ambiguity effectively. Commitment to the highest ethical, legal, regulatory, and scientific standards. Demonstrated professionalism, sound judgment, and scientific integrity. Passion for personal learning and professional development. Cultural sensitivity and adaptability within multinational organizations.

Physical Requirements

The role requires the ability to work in a field-based environment with frequent travel, including extended periods of sitting during air, ground, and other forms of transportation. The position may require pro