Medical Science Liaison

3 weeks ago


Canada Bristol-Myers Squibb Full time
Job Title: Medical Science Liaison - Cardiovascular

At Bristol-Myers Squibb, we are committed to transforming patients' lives through science. As a Medical Science Liaison - Cardiovascular, you will play a critical role in our mission by serving as a scientific liaison between Cardiology professionals and internal stakeholders.

Key Responsibilities:
  • Act as a scientific liaison between Cardiology professionals and internal BMS stakeholders through medical exchanges related to BMS products and associated therapeutic areas.
  • Ensure that data on BMS pipeline products is appropriately communicated in an efficient and timely manner through scientific exchanges.
  • Collect Medical insights & competitive intelligence.
  • Provide input into the Regional Field Medical plan.
  • Plan, organize and execute Regional Medical activities in collaboration with head office and field matrix teams.
  • Help to identify Investigator-Sponsored Research Trials (ISRs) as part of strategy development for the therapeutic area in Canada.
  • Keep abreast of key Cardiology treatment trends and emerging clinical science and ensure that this information is shared with appropriate BMS departments.
  • Ensure that all adverse drug events are reported in a timely and efficient manner as per BMS Policies & Directives.
  • Attend company and scientific meetings.
Requirements:
  • D. in life sciences. Two or more years of experience in biomedical sciences, pharmaceutical, drug information, clinical research or other related industry.
  • A Masters Degree in life sciences or health or equivalent could be considered if the candidate has a strong clinical experience or background in cardiology.
  • Strong scientific acumen especially in cardiology.
  • Ability to effectively communicate verbally and in writing, scientific/medical information to a diverse audience of both internal and external customers.
  • Understands clinical research in the field of Cardiology including Good Clinical Practices and ethical, governmental and regulatory requirements as they relate to clinical research and to the pharmaceutical industry.
  • Has the ability to understand and frame medical/research/scientific in relation to the specific constraints and requirements of the pharmaceutical industry.
  • Ability to manage multiple projects and unexpected issues that may arise.
  • Expected to travel 60% of the time with focus in Western provinces and must have a valid driver's license.
  • Must be able to communicate verbally and in writing in English.


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