Regulatory Affairs Associate Canada

Regulatory affairs professionals can support GSK submissions in Canada through hybrid work from Mississauga and flexible remote collaboration. Apply scientific knowledge to oncology-focused projects.This 12-month Regulatory Affairs Associate contract supports regulatory activities within a collaborative team environment. You will contribute to submissions, Health Canada communications, compliance, and project planning. The work requires knowledge of Canadian regulations, regulatory processes, and drug development.Key Responsibilities:
Provide input into submission and regulatory activity planningAssist with NDS, SNDS, CTA, and NC submissionsEnsure compliance with Health Canada and GSK guidelinesPrepare internal reports and Health Canada responsesCommunicate project plans and issues with global teamsRequirements:
Bachelor of Science in life science or related fieldSome regulatory affairs experienceUnderstanding of Canadian Food and Drug RegulationsKnowledge of regulatory requirements for submission typesExperience working with Veeva VaultBring regulatory planning, Canadian compliance knowledge, and scientific communication skills to GSK’s Mississauga team.
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