Clinical Drug Supply Chain Manager / Clinical Drug Supply Chain Manageress

Clinical Drug Supply Chain Manager - Contract - Cambridge, MA

What does it take to keep clinical trials running seamlessly from forecast to patient? If you're an expert in clinical supply chain management, we would love to hear from you.

Proclinical is seeking a Clinical Supply Chain Manager for a contract role based in the US.

Primary Responsibilities

The successful candidate will play a key role in forecasting investigational product (IP) supply requirements, managing distribution processes, and ensuring compliance with regulatory guidelines. This role involves collaboration with cross-functional teams and external partners to support clinical trials effectively.

Skills & Requirements

• Strong expertise in clinical supply management, including forecasting, inventory tracking, and distribution.
• Familiarity with IRT systems and their application in clinical trials.
• Ability to develop and oversee IP-related strategies, including expiry management and vendor coordination.
• Experience with budget management, RFPs, and vendor performance evaluation.
• Excellent communication and collaboration skills to work with cross-functional teams and external partners.
• Problem-solving abilities and knowledge of regulatory compliance standards.
• Relevant experience in the biotechnology or pharmaceutical industry, with a focus on clinical supply management.

Responsibilities of the Clinical Drug Supply Chain Manager

• Lead supply planning activities, including demand forecasting and alignment with study timelines.
• Manage IP inventory strategies, monitor usage trends, and define resupply activities.
• Oversee IP shipment orders to ensure timely and compliant delivery to investigator sites.
• Collaborate on the development and testing of Interactive Response Technologies (IRT) systems.
• Develop strategies for drug return, destruction, and resupply based on stability and shelf-life.
• Coordinate ancillary and comparator supply strategies with internal and external stakeholders.
• Provide input into IP-related study documents, tools, and training materials.
• Represent Clinical Drug Supply and Logistics on cross-functional study teams.
• Manage vendor relationships, budgets, and contracts for IP-related services.
• Track metrics, compile reports, and contribute to process improvement initiatives.

Apply online using the form below. Only applications matching the job profile will be considered.

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