About the job
Joining AbbVie means becoming part of an extraordinary team of professionals dedicated to making a significant impact on the lives of patients. At AbbVie, we engage in groundbreaking scientific research daily on a global scale. AbbVie Canada stands as one of the premier workplaces in the country.
As you chart your career path, choose to be exceptional.
AbbVie is committed to discovering and delivering innovative therapies to address critical health needs today and tackle tomorrow's medical challenges. We strive to make a remarkable difference in the lives of individuals across key therapeutic areas, including immunology, oncology, neurosciences, eye care, virology, women's health, gastroenterology, and aesthetics through Allergan Aesthetics products and services.
We are excited to announce an opening for a Medical Advisor to join our Medical Affairs team. This national role can be based in Montreal and reports to the Interim Medical Manager for Spasticity and Movement Disorders.
As a Medical Advisor, you will provide vital medical and scientific support to the clinical research service and participate in clinical operations activities. The Medical Advisor develops strategic plans that align with the brand plan and collaborates with various internal groups.
Key Responsibilities
- Develop a medical strategy within the brand team and implement this strategy in accordance with the brand plan.
- Support feasibility assessments, site mapping, clinical study determination, and ensure participation in clinical studies while resolving any outstanding site-related issues.
- Review new clinical study protocols and research proposals put forth by investigators.
- Maintain relationships with AbbVie Canada’s commercial teams, global project teams, researchers, and external experts by regularly reviewing ongoing initiatives and the tactical implementation of action plans.
- Provide scientific and medical support for ongoing projects.
- Monitor and review scientific documentation regarding AbbVie products and competitors.
- Act as a scientific affairs expert for the product.
- Serve as a liaison between medical affairs and commercial groups based on respective therapeutic areas.
- Ensure regulatory compliance in all conducted studies.
- Manage and allocate resources diligently, ensuring all project requirements are met.

