Medical & Scientific Liaison /Agent(e) de liaison médicale et scientifique

Get AI-powered advice on this job and more exclusive features. Territory: Eastern Ontario (up to Ottawa) Reporting to the National Medical & Scientific Liaisons Manager, the Medical & Scientific Liaison is a field‑based medical professional whose primary responsibility is to engage in non‑promotional peer‑to‑peer communication, using very strong interpersonal skills, and provide medical/scientific information to Scientific Leaders and Key Decision Makers based on cutting‑edge scientific exchange and services oriented towards the stakeholder’s professional interests and needs. Roles and Responsibilities Engage in non‑promotional peer‑to‑peer exchange of medical and scientific information with Scientific Leaders or Key Decision Makers to the extent permitted by law and local regulation, local industry codes, and the company's field medical standard operating procedure. Gain deep insights on disease, therapeutic area and healthcare needs, data gaps and challenges in the local geography. Represent Medical Affairs at local or regional non‑promotional medical events (e.g., medical congresses and symposia) and collaborate in the coordination of pre‑event scientific information and post‑event scientific summaries. Respond to unsolicited requests for medical, scientific, pipeline or marketed product information or indications from Scientific Leaders or Key Decision Makers utilizing appropriate approved scientific materials. Respond on a one‑to‑one basis to unsolicited requests for information on company research and/or grant activities by directing leaders to appropriate company resources for grants, sponsored clinical trial involvement, the Company’s Investigator Study Program, and outcomes research. Participate in Scientific Advisory Board meetings or Expert Input Forums when there is a defined role. Participate in the development of Medical Affairs Plans and implementation of activities identified in those plans. When requested by Global Clinical Trials Organization or Center for Observational and Real‑World Research personnel, support the identification of potential study investigators for sponsored studies. Qualifications Pharmacy Doctorate, PhD in Health Sciences (preferably related to the disease area) or Doctorate in Medicine. 2 to 3 years of industry experience and/or expertise in the related therapeutic area is preferred. Good knowledge of the therapeutic area (both basic and clinical literature). Demonstrated ability to acquire and maintain product, disease and competition knowledge. Language requirement: English. Strong interpersonal and communication skills. Budget management skills. Strong knowledge of company policies, procedures, industry standards, and applicable laws and regulations. Ability to analyze and understand the local community of practice. Ability to comprehend and integrate complex scientific concepts. Advanced knowledge of office technology and related software. Advanced analysis, planning, implementation and control skills. Advanced negotiation, presentation, and facilitation skills. Advanced project management skills. Must be located in the Greater Toronto Area or Eastern Ontario. Required Skills Adaptability Budget Management Cardiovascular Pharmacology Clinical Trial Methodology Clinical Trial Support Data Analysis Interpersonal Relationships Outcomes Research Pharmacology Project Management Relationship Building Scientific Communications Teamwork Therapeutic Knowledge Preferred Skills Current employees apply HERE Current contingent workers apply HERE We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal‑opportunity employer, committed to fostering an inclusive and diverse workplace. #J-18808-Ljbffr