Senior Clinical Supply Chain Operations Specialist

Real Staffing Group; Cambridge (MA); Hybrid; USD 53,000 - 76,000; Full time

Job summary

Pharmaceutical Company in Cambridge, MA is seeking a Senior Specialist, Clinical Supply Chain - Operations to ensure timely and compliant delivery of materials to sites and patients. The role focuses on day-to-day operations in a dynamic clinical trial environment.

You will lead end-to-end supply activities, coordinate with cross-functional teams, manage IRT-related tasks, and drive process improvements while maintaining inspection readiness. Hybrid contract in Cambridge, MA with a 6-month term.

Qualifications

• Bachelor's degree in Life Sciences or Supply Chain Management.
• At least 3 years of relevant clinical supply chain experience.
• Strong understanding of end-to-end clinical supply chain operations.
• Experience with IRT systems and CMOs.
• Knowledge of GxP and proficiency with Microsoft Office tools.
• Experience with Veeva is valued.

Responsibilities

• Lead end-to-end clinical supply execution for assigned studies, including packaging, labeling, distribution, inventory management, resupply, and study closeout.
• Align supply activities to protocol timelines and maintain visibility of inventory and supply availability.
• Partner with Clinical Operations, QA, Regulatory Affairs, and external vendors to support uninterrupted supply.
• Support IRT system activities for supply tracking and resupply execution.
• Identify and escalate operational risks and assist with investigations related to temperature excursions and supply deviations.
• Ensure accurate documentation and inspection readiness; contribute to process improvements and adoption of new tools and ways of working.

Skills

Clinical supply chain

IRT systems

GxP

Problem solving

Education

Bachelor's degree in Life Sciences or Supply Chain Management

Tools

MS Office

Veeva

Job description

Pharmaceutical Company in Cambridge, MA is seeking a Senior Specialist, Clinical Supply Chain - Operations to ensure timely and compliant delivery of materials to sites and patients. The role focuses on day-to-day operations in a dynamic clinical trial environment.

You will lead end-to-end supply activities, coordinate with cross-functional teams, manage IRT-related tasks, and drive process improvements while maintaining inspection readiness. Hybrid contract in Cambridge, MA with a 6-month term.