Regulatory affairs professionals can support GSK submissions in Canada through hybrid work from Mississauga and versatile 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 planning Assist with NDS, SNDS, CTA, and NC submissions Ensure compliance with Health Canada and GSK guidelines Prepare internal reports and Health Canada responses Communicate project plans and issues with global teams Requirements:
Bachelor of Science in life science or related field Some regulatory affairs experience Understanding of Canadian Food and Drug Regulations Knowledge of regulatory requirements for submission types Experience working with Veeva Vault Bring regulatory planning, Canadian compliance knowledge, and scientific communication skills to GSK’s Mississauga team.