Take the next step as a Regulatory Affairs Specialist for clinical trials and submissions in Canada and the US. Join our committed team in advancing medical science. We seek a Regulatory Affairs Specialist to enhance our efforts in regulatory and ethics submissions for clinical studies.

Your responsibilities will primarily include preparing dossiers, maintaining communication with relevant bodies, and ensuring quality control of submitted documents. Fluency in French and English is mandatory. Key Responsibilities:
Create and submit clinical trial documentation for regulatory bodies
Oversee translations of documents related to trial submissions
Provide regulatory training to project teams
Manage safety reporting for trial activities
Track progress of project documentation flow Requirements:
Bachelor’s degree or equivalent experience
Proven experience in clinical trial submissions in North America
Full proficiency in English and French, Spanish is advantageous
Detail-oriented with effective collaboration skills
Capacity to thrive in a rapid-paced team workplace Contribute to the vital processes that support creative health solutions across borders.

📌 Regulatory Affairs Specialist Canada/us Mississauga
🏢 PSI CRO
📍 Mississauga