Regulatory Data and Content Professional (Senior Medical Writer)

Work Location: This is an onsite role. Selected candidates will be required to work at the Mississauga Campus days every week.


Description:

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.

Creating a world where we all have more time with the people we love.

The Pharma Development Regulatory (PDR) is a flexible, bold, and distinctive regulatory organization. We make decisions quickly and strategically as the environment & landscape evolves.

We innovate. Within the PDR Data and Content Chapter, we are responsible for end-to-end data interpretation, generation and execution of content strategy, insight generation to guide submission strategy, and leadership of submission planning and management for clinical projects in the Client portfolio in order to develop and maintain Client product permits/licenses to meet...