Project Leader, Regulatory Development – Toronto with hybrid working – Global, top 10 Pharma - $competitive with excellent company benefits

The Company

• Global, top 10 Pharma company
• Hugely supportive team with a focus on employee wellbeing
• Covering multiple therapy areas
• Innovative R&D facilities

The Role

• RA project management of new and developed products
• Provide regulatory strategic and operational input to local and global teams for development and marketed products throughout their lifecycle.
• Develop and execute filing strategies.
• Assessing and summarizing scientific and clinical information.
• Organize and coordinate meetings with Health Canada.
• Ensure the preparation of high-quality regulatory submissions to meet agreed upon timelines and in compliance with Health Canada Regulations.
• Ensure the ongoing compliance for marketed products, specifically through product monograph and label updates/revisions.

You

• Minimum of 5 years of experience in Regulatory Affairs.
• Demonstrated success in a regulatory environment (e.g., leading a major submission).
• Good knowledge of the current Health Canada regulations and PAAB guidelines.
• Strong strategic and operational thinking
• Strong stakeholder management skills.

What should you do next?

This Project Leader, Regulatory Development role is one not to be missed; it encompasses the opportunity to work with a global, top 10 pharma company. To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.

If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.