Director, Clinical Supply Chain IRT

Role: Director, Clinical Supply Chain IRT, leading development and continuous improvement of IRT standards for clinical trials in oncology, including multiple Phase 3 studies for NSCLC and CRC. Responsibilities: serve as IRT process owner, design and optimize IRT solutions, ensure study start-up efficiency, compliance, scalable processes, and stakeholder collaboration across Clinical Supply Chain, Clinical Operations, Quality, and IT. Requirements: Bachelor’s in life sciences, supply chain, or related; 10+ years in Clinical Supply Chain, IRT/RTSM, or related biotech/pharma roles; strong knowledge of IRT design, testing, change control, and process documentation; proven stakeholder influence and process development skills; excellent communication and project management abilities. HighValue: extensive experience in IRT/RTSM systems, clinical trial operations, and process standardization; familiarity with regulatory compliance, validation, and scalable clinical supply chain processes in oncology; work involves cross-functional collaboration across global clinical programs. WorkSetup: onsite in Princeton, NJ or Palo Alto, CA; no travel specified.