Canadian Regulatory Affairs Consultant – Life-Cycle Management

We are seeking an experienced Regulatory Affairs professional with Canadian regulatory expertise to provide embedded support for the life-cycle management of five products currently marketed in Canada. This is an opportunity to work closely with the client’s regulatory organisation, providing hands-on support across routine regulatory submissions, complex regulatory activities, submission management and Health Authority interactions. Key Responsibilities Provide embedded Canadian Regulatory Affairs support across five marketed products. Lead the development and management of regulatory submissions, including routine submissions and supplements, as agreed with the client. Develop and execute regulatory strategies for complex submissions, ensuring appropriate regulatory pathways and approaches are identified. Act as the primary liaison with the Canadian Health Authority, coordinating interactions and supporting responses and follow-up activities. Manage submission activities throughout the regulatory lifecycle, including planning, coordination, review and delivery. Collaborate closely with the client’s dedicated RA CMC group, which is responsible for the CMC components of submissions. Coordinate cross-functional input and ensure regulatory deliverables are aligned, complete and submitted according to agreed timelines. Provide ongoing regulatory advice and support for the five products throughout their life-cycle management. Over the next 12 months, the portfolio is anticipated to include approximately: 2 efficacy supplements 6–8 CMC supplements The client has a dedicated RA CMC group responsible for the CMC submissions and associated activities. Experience & Skills Strong experience in Canadian Regulatory Affairs, ideally supporting marketed pharmaceutical products and life-cycle management. Demonstrated experience developing and managing regulatory submissions and supplements. Experience developing regulatory strategy for complex submissions. Proven ability to manage Health Authority interactions and act as a primary regulatory liaison. Strong project management and stakeholder coordination skills. Ability to work effectively as an embedded regulatory resource within an established client team. Experience collaborating with dedicated CMC regulatory teams is highly desirable. Excellent communication, organisational and problem-solving skills. Engagement Details Duration: 6–12 months Commitment: 35–40 hours per week Focus: Canadian Regulatory Affairs / Life-Cycle Management Portfolio: Five products currently marketed in Canada If you are an experienced Canadian Regulatory Affairs professional looking for an embedded consultancy assignment with significant submission and Health Authority engagement, we would be interested in hearing from you.

Provide embedded regulatory support for five marketed products in Canada, managing routine and complex submissions. Act as the primary liaison with the Canadian Health Authority and coordinate with the RA CMC group to ensure timely deliverables.

Requires strong experience in Canadian Regulatory Affairs and life-cycle management of pharmaceutical products. Must have a proven track record of managing Health Authority interactions and developing regulatory strategies for complex submissions.

• Project managementPreferred

Identified from the job description. Confirm important requirements above.

• Canadian Regulatory Affairs
• Life-Cycle Management
• Regulatory Submissions
• Health Authority Interactions
• Regulatory Strategy
• Submission Management
• Project Management
• Stakeholder Coordination
• CMC Collaboration
• Pharmaceutical Regulatory Compliance

• Consulting
• Healthcare
• Science & Research
• Manufacturing
• Legal

Minimum experience

5+ years

Posting language

English

Working hours

40 hours per week

Seniority

Mid-Senior level

Application method

Direct apply is available