Associate Clinical Supply Chain Management Specialist

Overview

In this role, you will enable successful clinical trials by applying IRT and clinical supply knowledge to design, configure, and optimize systems. You will work with cross-functional study teams to translate operational needs into system specifications, manage validation and testing, and drive process improvements. You will ensure quality, compliance, and efficient study delivery across global initiatives. This is an opportunity to advance clinical operations at scale within a data-driven, collaborative environment.

Responsibilities

• Design, set up, and maintain IRT solutions for clinical studies
• Translate study requirements into IRT specifications with stakeholders
• Contribute to risk assessments and support UAT for new setups and changes
• Review, develop, and execute testing and validation activities
• Provide guidance on IRT processes, systems, and best practices
• Partner with internal and external stakeholders for study startup, amendments, and ongoing management
• Support continuous improvement initiatives for IRT processes and tools
• Assist with training and knowledge sharing across study teams and functions
• Ensure activities comply with GCP and regulatory requirements

Key requirements

• Experience in clinical research, clinical supplies, clinical operations, or related biopharma environment
• Familiarity with IRT, RTSM, IVRS/IWRS or similar systems
• Strong analytical and problem-solving skills with multi-priority management
• Experience collaborating with cross-functional and global stakeholders
• Excellent communication and stakeholder management
• Strong attention to detail and quality mindset
• Proficiency with clinical systems and standard business applications

• communication
• stakeholder management
• problem-solving
• Interactive Response Technology (IRT)
• RTSM
• IVRS/IWRS

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