Work Location: This is an onsite role located within the Mississauga campus. Selected candidate is required to work at the Mississauga Campus minimum of three (3) times every week.

Role Summary The Global Clinical Distribution Team members have in-depth knowledge and understanding of clinical trial management, supply chain logistics, ERP systems and manage end-to-end distribution activities of a clinical study portfolio of varying complexity.

Our team members are globally distributed across Kaiseraugst, Switzerland, South San Francisco, U.S. and Mississauga (Greater Toronto Area), Canada.

As a member of the Study Management Chapter, you will manage the end-to-end distribution activities for a portfolio of clinical trials of varying complexity.

Your responsibility includes deploying clinical inventory throughout the global distribution network consisting of 24 depots worldwide from the point of technical release through importation and delivery of the clinical drug to depots and clinical sites.

The key responsibilities mentioned below highlight some focus areas; the actual role-based working setup may vary.

Global Clinical Distribution Lead (GCDL)

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

Mindset and Behaviors

You are action-oriented and can influence both internal and external stakeholders

You demonstrate curiosity, active listening, and a willingness to experiment and test new ideas when appropriate, focusing on continuous learning and improvement

You have a collaborative and agile mindset, actively looking to contribute to cross-functional teams and develop a self-directed team organization

You solve problems and can manage complex situations autonomously

You can manage multiple tasks and priorities

Required Experience and Education

Solid 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

AI Disclosure

This recruitment process will not use automated or AI-enabled tools to assist with application screening and scheduling. All hiring decisions are made by qualified human reviewers.

📌 RCI-RClinical Supplies Project Manager / Global Clinical Distribution Lead (Pharma/Biotech (Winnipeg)
🏢 Rangam
📍 Winnipeg