Medical Affairs Scientist

Baylis Medical Technologies • Mississauga, ON

5d • CA$70,000 - CA$90,000 • Hybrid

About The Position

The Medical Affairs Scientist plays a central role in advancing the organization's evidence-generation and dissemination strategy across the product lifecycle. Working in partnership with physicians, researchers, and key stakeholders, this individual enables and supports the development of high-quality clinical and scientific research aimed at addressing important clinical questions and unmet evidence needs. The role supports investigator-initiated studies, company-sponsored research (clinical and in vitro), registries, real-world evidence initiatives, health economics and outcomes research, and scientific publication activities. In addition to supporting external research collaborations, the Medical Affairs Scientist independently conducts scientific investigations, including systematic literature reviews, meta-analyses, publication deep-dives, white papers, scientific assessments, and bench or laboratory-based studies designed to generate novel insights and strengthen the evidence base.

Requirements

• Master's degree, PhD, MD, PharmD, or other advanced degree in life sciences, health sciences, biomedical engineering, epidemiology, public health, or a related scientific discipline.
• Demonstrated experience conducting independent scientific research through academic, clinical, industry, or post-graduate training environments.
• Strong understanding of research methodology, including study design, evidence evaluation, critical appraisal of literature, and scientific inquiry.
• Experience conducting literature reviews and synthesizing scientific evidence from multiple sources.
• Excellent scientific writing skills, with the ability to prepare reports, evidence summaries, manuscripts, abstracts, presentations, and other scientific communications.
• Strong analytical and problem-solving skills, with the ability to interpret complex scientific, clinical, and technical information.
• Proficiency in data analysis, including experience with statistical methods and data interpretation.
• Exceptional verbal, written, and interpersonal communication skills, with the ability to communicate effectively with physicians, researchers, and cross-functional stakeholders.
• Highly organized with strong attention to detail and the ability to manage multiple projects and deadlines simultaneously.
• Self-motivated, intellectually curious, and capable of working both independently and collaboratively in a dynamic environment.

Nice To Haves

• Experience in body and neuro interventional space
• Authorship or significant contributions to peer-reviewed publications, scientific presentations, abstracts, white papers, theses, or technical reports.
• Familiarity with statistical software, literature review tools, reference management software, and scientific databases.
• Exposure to regulated environments (e.g., medical device, pharma)

Responsibilities

• Contribute to the development and execution of evidence-generation strategies across the product lifecycle, including clinical, in vitro, real-world, health economic, and post-market research initiatives.
• Identify evidence gaps, emerging trends, and opportunities for research through literature review, scientific landscape assessments, stakeholder engagement, and data analysis.
• Support investigator-initiated studies, company-sponsored research, registries, real-world evidence studies, and bench or laboratory-based research.
• Partner with physicians, investigators, and researchers to develop research concepts, study protocols, analysis plans, abstracts, manuscripts, and scientific presentations.
• Independently conduct scientific investigations, including systematic literature reviews, meta-analyses, publication deep-dives, evidence assessments, white papers, and scientific dossiers.
• Analyze and interpret clinical, scientific, bench, and real-world data to generate insights, support evidence development, and inform scientific strategy.
• Translate complex scientific information into clear and impactful scientific communications, including reports, publications, presentations, evidence summaries, and educational materials.
• Contribute to publication planning and execution, including congress submissions, peer-reviewed manuscripts, posters, podium presentations, and other evidence dissemination activities.
• Monitor scientific literature, clinical practice trends, guidelines, and competitive evidence to inform research priorities and evidence strategies.
• Serve as a scientific resource to internal stakeholders by providing research-based insights that support innovation, product development, medical education, reimbursement, and commercialization activities.
• Collaborate with cross-functional teams including R&D, Regulatory, and Marketing to ensure evidence is effectively generated, interpreted, and disseminated.
• Maintain high standards of scientific rigor, documentation, data integrity, compliance, and ethical conduct in all activities.
• Stay current with relevant disease states, research methodologies, and scientific advancements.
• Travel occasionally to support scientific conferences, investigator meetings, research collaborations, and other stakeholder engagements.
• Comply with company Health & Safety policies and perform other duties as required.
• Other duties as required

Benefits

• Complimentary shuttles
• Subsidized transit options
• Flexible working approach
• One dedicated day off for volunteering
• Access to training, workshops, and development opportunities
• Comprehensive total rewards package including health spending account and tuition support
• Vibrant workplace culture with employee-led clubs, activities, and events

What This Job Offers

• Job Type: Full-time
• Career Level: Senior