Associate Medical Director, Global Drug Safety
- Mississauga, ON
- Hybrid
- Posted Sep 12, 2026
- 1 position
$123,960–$162,698 / year
Opens an external site
- Employment type
- Full-time
- Experience level
- Mid-level · 2+ years
- Minimum education
- Master’s degree
- Apply by
- Oct 9, 2026
- Posting language
- English
- Working hours
- 40 hours per week
- Office presence
- 3 days per week
Job summary
The Associate Medical Director manages safety and risk management activities for clinical development projects and marketed products. They are responsible for identifying safety signals, conducting medical reviews of safety reports, and contributing to core regulatory documentation.
Job details
The Associate Medical Director manages safety and risk management activities for clinical development projects and marketed products. They are responsible for identifying safety signals, conducting medical reviews of safety reports, and contributing to core regulatory documentation. Candidates must hold an MD or equivalent degree and possess knowledge of US and EU safety regulations. Experience in drug safety and risk management within the pharmaceutical, biotech, or CRO industry is preferred.
What you’ll do
The Associate Medical Director manages safety and risk management activities for clinical development projects and marketed products. They are responsible for identifying safety signals, conducting medical reviews of safety reports, and contributing to core regulatory documentation.
Requirements
Candidates must hold an MD or equivalent degree and possess knowledge of US and EU safety regulations. Experience in drug safety and risk management within the pharmaceutical, biotech, or CRO industry is preferred.
Benefits
- Flex Benefits
- Retirement Savings Program
- Paid Vacation
- Personal Days
- Variable Pay Bonus
- Short Term Incentive
- Equity-based Long-term Incentive
Listed skills
- Time management · Preferred
- Problem solving · Preferred
- Regulatory Compliance · Preferred
- Data analysis · Preferred
- Risk Management · Preferred
- Communication · Preferred
- Project management · Preferred
- Cross-Functional Collaboration · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Drug Safety
- Risk Management
- Pharmacovigilance
- Regulatory Compliance
- Medical Review
- Signal Detection
- Clinical Development
- Data Analysis
- Project Management
- Regulatory Reporting
- Labeling Documentation
- Cross-functional Collaboration
- Problem Solving
- Communication
- Time Management
Job areas
- Healthcare
- Science & Research
- Management & Leadership