Bedrocan-Regulatory Affairs Associate Regulatory Affairs Associate, Medical - Toronto, ON
Candidate will be responsible for the preparation and compilation of dossiers for regulatory submissions and registration of Canopy drug development activities in Canada. This involves strategizing, planning, managing, writing, and/or reviewing clinical activities and documents for all aspects of the regulatory submissions. Strong links need to be established with all Canopy departments involved e.g. Medical and Research, IT, and specifically all external partners to ensure dossiers are prepared, compiled and maintained in compliance with the regulations and are submitted and approved in an efficient and timely manner.