Medical Affairs Scientist at Baylis Medical Technologies — NeverHard

The Big Picture 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. Your Impact Through Innovation 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. Required Skills 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. Preferred Skills 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). Our Distinctive Edge Effortless commute: complimentary shuttles and subsidized transit options. Work‑life integration: flexible working approach to support balance and performance. Making a difference: one dedicated day off for volunteering to support causes you care about. Nurturing your career: access to training, workshops, and development opportunities. Rewards that count: comprehensive total rewards package including health spending account and tuition support. Unleash your spirit: be part of a vibrant workplace culture with employee‑led clubs, activities, and events. Our Impact Baylis Medical Technologies is a leader in the development and manufacturing of innovative medical devices in the fields of radiology and cardiovascular interventions. Headquartered in Canada, the company also provides contract manufacturing services to some of the world’s leading medical device companies. Baylis Medical Technologies is an equal‑opportunity employer and encourages applications from all qualified individuals. Please inform us if you require any accommodations during the recruitment process. This role has a base salary range of $70,000 CAD to $90,000 CAD. Final offers are determined based on individual skills, experience, qualifications, location, and other job‑related factors. #J-18808-Ljbffr