Non-Clinical Toxicology Program Lead

Alexion Pharmaceuticals, Inc.

Mississauga

Hybrid

CAD 111,000 - 146,000

Full time

6 days ago
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Benefits offered by this job

4 weeks paid vacation
Annual Personal Days
Flex Benefits
Retirement Savings Plan
Equity-based long-term incentive

Job summary

Alexion Pharmaceuticals, Inc. in Mississauga, Ontario seeks a Non-Clinical Manager to lead preclinical studies and collaborate with global teams, CRO partners, and regulatory affairs.

You will oversee study design, implementation, and reporting across pharmacokinetics, toxicology, and safety pharmacology. The successful candidate will bring deep scientific knowledge, strong project management, and excellent communication skills to ensure timely, compliant studies within budget.

Qualifications

  • PharmD, VetD, or master’s in biology/toxicology; or BA/BS with relevant experience.
  • 3–5 years of toxicology study director/monitor experience in pharma/biotech/CRO.
  • GLP fundamentals and data interpretation of nonclinical studies.

Responsibilities

  • Select partners for studies based on expertise, quality, cost, and time.
  • Liaise with CROs for contracts, invoices, study setup, monitoring, and reporting.
  • Identify and resolve scientific, technical, logistical, or quality issues.
  • Ensure studies meet regulatory and quality requirements.
  • Review and interpret data; coordinate report review with high quality standards.
  • Summarize results to project teams and management.
  • Coordinate activities with finance, CMC, bioanalysis, regulatory, etc.
  • Monitor developments in your field of expertise.

Skills

English proficiency
Project management
Communication skills
Attention to detail
Budget management

Education

PharmD/VetD/Master’s in biology/toxicology

Job description

Alexion Pharmaceuticals, Inc. in Mississauga, Ontario seeks a Non-Clinical Manager to lead preclinical studies and collaborate with global teams, CRO partners, and regulatory affairs.

You will oversee study design, implementation, and reporting across pharmacokinetics, toxicology, and safety pharmacology. The successful candidate will bring deep scientific knowledge, strong project management, and excellent communication skills to ensure timely, compliant studies within budget.

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