Global Clinical Distribution Lead
- Mississauga, ON, Canada
$40 to $46 CAD / hour · Contract
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Job details
- Pay
- $40 to $46 CAD / hour
- Job type
- Contract
- Apply by
- Experience
- 2-4 years’ experience in Clinical Trial Management, logistics, warehouse management, or other Supply Chain disciplines, preferably in the Biotechnology / Pharmaceutical industry
- Posting language
- English
- Posted
Original job description
Job Responsibilities
- As a Global Clinical Distribution Lead, you will play a variety of roles according to your experience, knowledge, and general business/team requirements, such as:
- Manage the On-time Delivery Performance for network supply shipments in the distribution network to meet study requirements and patient demand
- Effective participation and engagement on Protocol Execution Teams (PETs), Global Supply Execution Teams (gSETs), and ad-hoc distribution-related meetings on behalf of PTDS
- Drive resolution of operational and system matters impacting on-time delivery collaborating with providers internal and external
- Execute and coordinate network depot supply in coordination with the Clinical Demand and Supply Leader and other partners as needed
- Lead and participate in cross-functional and internal distribution-related projects and process improvement initiatives supporting the global distribution and PTDS strategy
- Execute with the highest level of accuracy in the CLARA system and perform 1st and 2nd-level diagnostics
- Operate within a GMP-compliant environment, ensuring adherence to quality procedures in place
- Processing event records such as quality incidents as well as CAPAs and Changes (Planned Events) if applicable
Required Experience and Education
- Strong SAP / ERP systems knowledge and experience
- Experience in cross-functional/cross-cultural and agile organizational models
- 2-4 years’ experience in Clinical Trial Management, logistics, warehouse management, or other Supply Chain disciplines, preferably in the Biotechnology / Pharmaceutical industry
- Degree (BA, BS, MS, MBA) in Business (Operations Management or Supply Chain Management), Biotechnology or relevant field
- APICS and/or SCOR certification a plus
- Operational Excellence/ Six Sigma/ Lean training a plus
More about this job
Responsibilities
Manage on-time delivery of clinical trial supplies, coordinate depot supply, and resolve operational or system issues with internal and external partners. Participate in cross-functional teams and improvement projects, maintain accurate CLARA system records, and ensure compliance with GMP and quality procedures.
Requirements
Candidates should have 2–4 years of experience in clinical trial management, logistics, warehouse management, or another supply chain discipline, preferably in biotechnology or pharmaceuticals, along with strong SAP or ERP systems experience. A degree in business, biotechnology, or a related field is required; APICS or SCOR certification and training in Operational Excellence, Six Sigma, or Lean are advantages.
Skills
- Clinical Trial Management
- Clinical Distribution
- Supply Chain Management
- Logistics
- Warehouse Management
- SAP
- ERP Systems
- On-Time Delivery Performance
- Depot Supply Coordination
- Cross-Functional Collaboration
- Protocol Execution
- GMP Compliance
- Quality Incident Processing
- CAPA Management
- Operational Excellence
- Lean
Visa sponsorship
Not detected in the job text
Categories
- Logistics
- Healthcare
- Management & Leadership
Keywords
- Clinical Trial Management
- Clinical Distribution
- Supply Chain
- Logistics
- Warehouse Management
- Biotechnology
- Pharmaceutical Industry
- SAP
- ERP Systems
- CLARA System
- On-Time Delivery
- Network Depot Supply
- Protocol Execution Teams
- Global Supply Execution Teams
- GMP Compliance
- Quality Procedures
- Quality Incidents
- CAPA
- Planned Events
- Cross-Functional Collaboration
- Cross-Cultural Teams
- Agile Organizational Models
- Process Improvement
- Operational Excellence
- Six Sigma
- Lean
- APICS
- SCOR