Intern, Clinical Supply Chain

The Opportunity:

This internship provides foundational training in clinical supply chain operations, documentation practices, and systems used to support global clinical trials. The intern will develop a working understanding of how supply chain activities directly impact study execution, compliance, and patient safety. As a Clinical Supply Chain Intern, you will gain hands-on exposure to the operational backbone that supports global clinical trials. You will work closely with the Clinical Supply Chain team to understand how investigational product (IP) is planned, documented, distributed, and maintained in compliance with GxP and regulatory standards.

By the end of the internship, the intern will be able to:

• Understand the role of clinical supply chain in clinical trial execution.

• Identify key elements of batch documentation relevant to clinical supply.

• Understand temperature excursion processes and documentation requirements.

• Review depot-level shipment documentation for completeness and compliance.

• Organize and centralize shipment documentation within a TMF structure.

• Apply GxP principles and inspection-ready documentation practices.

Required Skills, Experience and Education:

• Currently pursuing a degree in Supply Chain, Life Sciences, Pharmacy, Engineering, or related field.

• Interest in biotechnology, pharmaceutical operations, or clinical development.

• Strong attention to detail and organizational skills.

• Proficiency in Microsoft Excel and general document management tools.

• Strong communication skills and willingness to learn in a regulated environment.

• Excellent organizational, communication, and problem-solving skills.

• Ability to work independently while collaborating effectively across functions and with external partners. 

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