Job Description
📋 Description Support planning, execution, and optimization of clinical trial supply activities. Collaborate with Clinical Operations, Regulatory, Quality, CMC, CMOs and IRT vendors. Develop supply plans, inventory strategies, production schedules, and risk mitigation. Monitor production schedules, identify issues, and support corrective actions. Coordinate label management and ensure regulatory compliance. Support comparator sourcing and IRT system activities. 🎯 Requirements Bachelor’s degree or higher in life sciences, supply chain or related field, or equivalent 2+ years in supply chain, preferably in biotech/pharma/CRO/clinical research. Understanding of clinical trial supply, inventory, labeling, packaging, and distribution. Strong analytical, organizational, and cross-functional collaboration skills. Proficiency with Microsoft Word, Excel, and Outlook. Ability to work in a fast-paced environment and adapt to changing priorities. 🎁 Benefits Competitive annual salary USD 79,100 - 109,100, depending on skills and location. Eligibility for annual bonus, equity awards, and employee stock purchase program. Comprehensive medical, dental, vision, 401(k), FSA/HSA options. Life insurance and paid time off with wellness benefits. Collaborative, growth-focused environment in global clinical development.
