Senior Clinical Drug Supply Manager

Role: Senior Clinical Trial Drug Supply Manager overseeing global supply chain operations for clinical trials, primarily in oncology and neurological indications. Responsibilities include demand forecasting, supply planning, inventory management, packaging, labeling, distribution, and compliance with GCP, GMP, and GDP standards. The role involves coordinating with external vendors, managing logistics, supporting supply system configurations (IRT/IVRS), and ensuring uninterrupted drug availability at multiple sites. Leadership duties include mentoring supply chain professionals and driving process improvements. Qualifications: Bachelor’s degree in Life Sciences, Pharmaceutical Sciences, or related field; 8+ years in pharmaceutical/biopharmaceutical clinical supply, with experience supporting multi-phase, global trials and familiarity with oncology programs. Expertise needed in supply forecasting, distribution, regulatory compliance, and clinical trial systems such as IRT/CTMS. Preferred skills include strong project management, stakeholder communication, and proficiency with supply chain IT platforms. High-value specifics: Oncology and neurology trial support, GxP compliance, global logistics, regulatory documentation, and cross-functional collaboration across Clinical Operations, Regulatory, Quality, and Manufacturing. Work setup: Not specified, but involves global coordination and stakeholder interaction.