Senior Clinical Supply Chain Operations Specialist

Planet Pharma; Cambridge (MA); On-site; USD 58,000 - 66,000; Full time

Job summary

Planet Pharma in Cambridge, MA is seeking a Specialist, Clinical Supply Chain – Operations to ensure reliable and compliant execution of clinical supply across protocols, delivering materials to sites and patients on time. You will manage end-to-end supply activities, work with Clinical Ops, QA, Regulatory, and external vendors, and support IRT systems, CMOs, and temperature excursion investigations.

Requires a BS in Life Sciences or SCM and 3+ years of experience, MS Office skills, attention to

Qualifications

• 3+ years of relevant experience in clinical supply
• Experience with end-to-end supply chain activities in a clinical setting
• Strong communication and collaboration across stakeholders

Responsibilities

• Lead end-to-end execution of clinical supply activities including packaging, labeling, distribution, inventory management, and study closeout
• Align supply activities to protocol timelines (site readiness, patient supply, resupply)
• Maintain visibility to inventory levels and supply availability across studies
• Partner with Clinical Operations, QA, Regulatory, and vendors to execute supply plans
• Support management of IRT systems for supply tracking and resupply
• Identify and escalate execution risks such as delays or deviations
• Support investigations of temperature excursions and supply deviations
• Ensure activities are compliant, documented, and inspection-ready
• Contribute to process improvements and tool adoption
• Maintain documentation including supply plans and trackers

Skills

End-to-end supply understanding

Strong communication

Attention to detail

Multi-tasking

Education

BS in Life Sciences or Supply Chain Management

Tools

MS Office Suite (Excel, PowerPoint, Visio, Project)

Job description

Planet Pharma in Cambridge, MA is seeking a Specialist, Clinical Supply Chain – Operations to ensure reliable and compliant execution of clinical supply across protocols, delivering materials to sites and patients on time. You will manage end-to-end supply activities, work with Clinical Ops, QA, Regulatory, and external vendors, and support IRT systems, CMOs, and temperature excursion investigations.

Requires a BS in Life Sciences or SCM and 3+ years of experience, MS Office skills, attention to