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Umoja Biopharma · 3 days ago

Senior Specialist, Clinical Supply Chain

Louisville, CO

Full-time

Hybrid

Senior Level, Lead/Staff

$107K/yr - $132K/yr

8+ years exp

Umoja Biopharma is an industry-leading biotech focused on transforming cancer treatment with a novel immunotherapy platform. The Senior Clinical Supply Chain Specialist will support Clinical Supply Chain activities, ensuring compliant supply of clinical materials and collaborating with various internal and external stakeholders.

BiopharmaBiotechnology

Responsibilities

Clinical Supply Planning – develop supply plans and strategies to ensure on-time supply to clinical sites based on clinical forecasts, identify, mitigate, and resolve supply chain risks, issues, and recall support

Logistics and Distribution – work with third party logistic provider to manage domestic and global distribution

Third Party Logistic Provider (3PL) management – oversee label, pack, and distribution activities at 3PL, responsible for contract management, including contract approval, budget, and invoicing

Compliance – ensure adherence to GMP regulations as required, generate and maintain applicable SOPs and shipment tracking

Cross-functional collaboration – work closely with Clinical Operations, External Quality, Regulatory, and Finance as required

Be a champion for policy, process, and compliance for all GMP-related procurement and clinical supply chain activities

Assist the Supply Chain Team with additional responsibilities in support of shipping/logistics and/or material resource planning as needed

Qualification

Clinical Supply ChainLogistics ManagementGMP ComplianceThird Party LogisticsERP SystemsMicrosoft OfficeCommunication SkillsDetail OrientedProblem SolvingSelf-Motivated

Required

Bachelor's degree in science, engineering, business or a related discipline and a minimum of 8 years of relevant industry experience in business operations role, or an equivalent combination

Minimum of 5 years of clinical supply chain/supply chain, logistics, and/or operations-related experience in a cGMP environment

Working knowledge of Clinical Supply Chain activities and strategies

Experience working in a regulated manufacturing environment; pharmaceutical or biotechnology

Detail oriented with the ability to identify and solve complex problems with minimum assistance

Self-motivated, pro-active, and able to work well both on a team and independently

Strong communication skills are a must