Job Title

Our client is a Toronto-based innovator in the medical device and imaging industry, developing advanced diagnostic solutions that transform patient care and wound management worldwide. Reporting to the Director of Clinical Trials & Education, the Medical Communications Director (MCD) is responsible for building and managing the body of clinical evidence that defines the value and competitive positioning of the companys technology. This role translates complex clinical data into clear, compelling messages for internal and external stakeholders, supporting product adoption, marketing, reimbursement, and regulatory objectives. The MCD also drives the publication strategy, engages with key opinion leaders (KOLs), and ensures the timely dissemination of high-quality scientific content. Responsibilities Clinical Evidence Ownership: Maintain and analyze the publication portfolio, identify gaps and opportunities, and serve as the subject matter expert across marketing, reimbursement, regulatory, and quality. Publications & Dissemination: Oversee the creation of manuscripts, abstracts, posters, and presentations; ensure timely, high-quality dissemination of clinical data; and foster KOL and investigator relationships. Cross-Functional Support: Provide clear, evidence-based messaging for internal stakeholders, ensuring scientific accuracy and alignment with business objectives. Conferences & External Engagement: Identify and prepare KOL speakers, manage congress submissions, and represent the organization at key scientific and industry forums. Operational Excellence: Drive quality control, compliance, and process improvements, while managing projects and medical writers to successful, on-time completion. Qualifications Postgraduate degree in a scientific, health, or medical communications field (MSc, PhD, MD, PharmD). 5+ years of experience in medical communications and scientific writing, including peer-reviewed publications. Proven ability to lead publication strategies and collaborate across cross-functional teams and clinical partners. Strong project management, organizational, and communication skills with high attention to detail. Proficiency with MS Office, reference management tools, and scientific presentation design. Familiarity with diagnostics, imaging, microbiology, or regulatory environments preferred. If you think this is something that aligns with your experience, reach out to me directly at #J-18808-Ljbffr