Contribute to the advancement of clinical supplies by ensuring compliance and quality for crucial batch disposition activities. Partner with cross-functional teams to manage risks and improve processes, guaranteeing uninterrupted access to trials.

Accelerate clinical development by managing trial design, execution, and data analysis in a dynamic, cross-functional team environment, ensuring compliance with regulatory standards and delivering high-quality scientific insights for product strategy.

Unlock potential by driving scientific engagement with key experts in Eye Care. As a Medical Science Liaison, you'll build relationships and provide critical insights to advance our mission within the Quebec territory, fostering credibility and collaboration.

Join a team that enhances medical writing operations, ensuring the quality and compliance of clinical documentation through expert quality control, mentorship, and collaboration across research and regulatory functions.

Play a key role in advancing scientific credibility through expert relations and presentations, while supporting clinical studies in the eye care therapeutic area, covering the Quebec territory. Travel required about 50%.