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 setting. 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.

📌 Regulatory Affairs Associate Canada (Mississauga)
🏢 GlaxoSmithKline
📍 Mississauga