QUALIFICATIONS:

· Completion of either a BSc or equivalent education
· Experience relating to project management
· Completion of Accredited GMP courses are an asset
· Experience relating to quality assurance is an asset
· Relevant clinical trials experience preferred

ADDITIONAL SKILLS, KNOWLEDGE AND/OR ABILITIES:

· Strong interpersonal and collaboration skills across various departments and stakeholders.
· Excellent verbal and written communication skills.
· Proficient in MS Office Suite.
· Strong organizational and multitasking abilities.
· Quick learner with the ability to absorb and apply information effectively.
· Proactive, detail-oriented, and adaptable to shifting priorities.
Job Type: Full-time
Pay: From $50,000.00 per year

Benefits:

• Company pension
• Dental care
• Disability insurance
• Employee assistance program
• Extended health care
• Life insurance
• On-site parking
• Paid time off
• Vision care

Ability to commute/relocate:

• Dundas, ON L9H 7P3: reliably commute or plan to relocate before starting work (required)

Education:

• Bachelor’s Degree (preferred)

Work Location: In person
Application deadline: 2025-08-3

· Develop and prepare processes relating to receiving materials, clinical trial packaging, labeling, storing, and distribution. Document all packaging material specifications, detailed packaging directions, descriptions and requirements from the CTC.
· Assist in writing technical procedures and Standard Operating Procedures.
· Conduct in-process checks to ensure procedures are accurately performed by all staff in the Clinical Trial Packaging area during packaging and labeling procedures.
· Participates in discussions with sponsors, investigators and other parties as necessary regarding all aspects of the Clinical Trial Agreement.
· Directs and trains Logistics/Packaging Technicians in the preparation/packaging of study medications and in all necessary study specific duties.
· Assists in providing information for routine audits of all functions to ensure compliance of all procedures.
· Works with purchasing staff and Quality to establish quality requirements for external suppliers.
· Adheres to established standards of service for customers or clients.
· Ensure compliance with environmental and health/safety standards.
· Accurately monitor clinical trials supplies/inventory, as required.
· May be required to perform other tasks or duties, as assigned.