Global Clinical Distribution Lead

Fuze HR Solutions; Mississauga; On-site; CAD 100,000 - 120,000; Full time

Job summary

A recruitment agency is looking for a Global Clinical Distribution Lead in Mississauga, Ontario. This onsite role requires at least 3 days a week attendance and offers a salary of $100,000-$120,000. The ideal candidate will have over 3 years of experience in supply chain management and logistics, particularly in clinical distribution. The position involves coordinating the distribution of clinical trial materials globally and requires knowledge of SAP and international shipping regulations. Comprehensive training is provided.

Qualifications

• 3+ years of hands-on experience in supply chain, logistics, or clinical distribution.
• Experience with temperature-controlled transportation and logistics.
• Strong knowledge of customs regulations and international shipping requirements.

Responsibilities

• Coordinate end-to-end distribution of clinical trial materials across multiple countries.
• Ensure timely delivery while managing lead times and regulatory requirements.
• Collaborate with global study teams and external service providers.

Skills

Supply chain management

Logistics coordination

Attention to detail

Strong organization

Problem-solving

Collaboration

Tools

SAP

Job description

Global Clinical Distribution Lead

Location Mississauga, Ontario
(Onsite role – minimum 3 days per week required)

Compensation $100,000-$120,000

Schedule

• Full-time: 40 hours per week
• 8-hour workdays
• Long-term contract (with potential to become permanent)

Start date: As soon as possible!

About the Role

We are seeking a Global Clinical Distribution Specialist to join a dynamic and fast-paced supply chain team supporting clinical trial distribution activities worldwide. This role is highly administrative and operational, requiring strong organization, attention to detail, and the ability to work strategically in a high-pressure, global environment.

The position supports increasing volumes and offers long-term career growth within the supply chain function.

Key Responsibilities

• Coordinate end-to-end distribution of clinical trial materials across multiple countries.
• Ensure timely delivery while managing lead times, transportation constraints, and regulatory requirements.
• Collaborate with global study teams, internal stakeholders, and external service providers.
• Support distribution activities across temperature-controlled transportation networks.
• Work closely with logistics partners and third-party vendors (e.g., courier and freight providers).
• Manage data accuracy across enterprise systems, including SAP and other IT platforms.
• Support process improvements, automation initiatives, and manual operational workflows.
• Navigate varying international regulations and distribution requirements across regions.
• Assist with issue resolution related to supply chain disruptions, system challenges, and volume increases.
• Operate in a GMP-compliant environment and follow quality standards and procedures.

Qualifications & Experience

• Minimum 3 years of hands‑on experience in supply chain, logistics, or clinical distribution (more is strongly preferred).
• Background in clinical trial supply chain or pharmaceutical distribution is a significant advantage.
• Experience in temperature‑controlled transportation and logistics.
• Strong working knowledge of SAP and complex IT environments.
• Familiarity with customs regulations and international shipping requirements (not a customs broker role).
• Experience working in global, cross‑functional environments with diverse stakeholders.
• Exposure to logistics, pharma, or clinical research organizations is highly valued.

Preferred Experience

• Clinical distribution within the pharmaceutical or biotech industry.
• Supply chain roles supporting clinical studies.
• Experience in organizations undergoing system changes (e.g., SAP implementations).
• Understanding of regulatory and distribution challenges across multiple countries.
• Pharma background is a strong asset; clinical experience is especially valuable.

Additional Information

• Comprehensive onboarding and training program provided (systems, processes, and compliance).
• Role involves high accountability and strict delivery timelines.
• Two‑round interview process, with final discussions involving leadership.

To apply email your resume to [e-mail]