About The Position

Medical Scientific Liaisons (MSLs) are responsible for engaging in non-promotional, peer-to-peer communications and providing medical/scientific information to Scientific Leaders (SLs) and Key Decision Makers (KDMs). The incumbent will demonstrate strong ethics and a solid understanding of the environment governing our industry as he/she will be expected to complete his/her tasks in a manner fully consistent with Organon’s Code of conduct, policies, procedures, industry standards and all laws and regulations.

Requirements

  • Strategically, and consistently demonstrates the capability of applying up to date essentials of scientific knowledge at a peer-to-peer level across the scientific engagement model (SEM)
  • Strategically and consistently demonstrates the capability of peer-to-peer scientific exchange across the SEM; while providing back information to internal stakeholders via organization systems thoroughly strategically and consistently.
  • Strategically and consistently demonstrates the capability of research support across the SEM; while leveraging the internal systems and executing in a manner that meets the organizational needs.
  • Strong scientific baseline knowledge in assigned therapeutic area(s).
  • Strong knowledge about clinical trial methods, implementation, and data interpretation.
  • Sound scientific understanding, and eagerness to continue learning about a specific therapeutic area.
  • Ability to present scientific and other technical information with confidence, in a way that engenders trust and credibility.
  • Excellent communication skills, including listening and probing skills, across a variety of internal and external audiences.
  • Strong collaboration skills and ability to function within a team environment.
  • Ability to handle multiple tasks at the same time and work under pressure
  • Degree in medicine (MD), Doctorate in health sciences (PhD), Degree in pharmacy (PharmD), or a Master of Science (MSc)
  • Strong knowledge of company policies, procedures, industry standards, as well as applicable laws and regulations
  • Ability to travel extensively (up to 50% of working time)
  • Fluency in English and French, with strong verbal and written communication skills in both languages, is required as the incumbent will interact with SLs and KDMs in Ontario, Québec and the Atlantic region.

Nice To Haves

  • Experience in the pharmaceutical industry is an asset
  • Knowledge and experience in migraine therapeutic area is an asset

Responsibilities

  • Engage in non-promotional, peer-to-peer exchange of medical and scientific information with SLs or KDMs to the extent permitted by law and local regulation, local industry codes, and other provisions of the Guiding Principles for Global Standard Ex-US Field Medical Activities.
  • Gain deep insights on disease, therapeutic area and healthcare needs, data gaps and challenges in their local geography.
  • Represent Medical Affairs at local or regional non-promotional Medical events (e.g. Medical Congresses and Symposia) — may 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 SLs or KDMs, utilizing appropriate approved scientific materials.
  • Respond to unsolicited requests for information on company research and/or grant activities by directing SLs or KDMs to appropriate company resources for grants, sponsored clinical trial involvement, and outcomes research.
  • Organize and participate in medical and scientific exchange activities, which include but are not limited to learning activities, expert input forums, and advisory boards.
  • Share, on a reactive basis, the publicly available areas of interest with SLs and direct them to the appropriate resources for further information.
  • Formulate regional Medical Affairs Plans and implement its activities.
  • Support the identification of potential study investigators for sponsored studies, at the request of the clinical trials organization personnel.
  • Provide insights on the scientific gaps, ideas and other topics gathered from scientific exchange to inform areas of interest, development programs, and company strategy.
  • Support company commercial colleagues by providing on-label or disease state scientific training, when requested and where allowed.

Benefits

  • Flex Time
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