Global Clinical Distribution Lead in Mississauga

Duration: 12 months (possible extension)

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

Client is a global pioneer in pharmaceuticals and diagnostics, focused on advancing science to improve people’s lives. As the world's largest biotech company and a global leader in in-vitro diagnostics, Client is committed to driving innovation and delivering personalized healthcare. We thrive on a culture of intellectual curiosity and diversity, where every individual is empowered to make a significant impact on patients' lives worldwide.

The Global Clinical Supply Chain Organization’s objective is to cost-effectively ensure the right product is in the right place at the right time every time, such that no patient will go without treatment and no clinical trial will be delayed. Our vision is to enable an adaptive Supply Chain delivering innovative and sustainable clinical supply solutions anytime, anywhere, to anyone.

As a part of our team, you will directly contribute to the success of Client’s robust and diverse pipeline of biopharmaceuticals, as our team is accountable for the Clinical Supply of more than 100 molecules in 600+ clinical trials across seven disease areas. 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.

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.

Job Responsibilities:

• 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:

• 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.