Clinical Supplies Manager

• Responsibilities

  - Develop and execute clinical supply strategies for multiple global studies. - Forecast supply needs based on enrollment projections and protocol requirements. - Coordinate with manufacturing, packaging, labeling, and logistics teams to ensure timely availability of materials. - Manage vendor relationships, including contract negotiations and performance monitoring. - Ensure compliance with Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), and all applicable regulatory guidelines. - Oversee inventory control systems to track product quantities, expiry dates, and distribution records. - Implement risk mitigation strategies to prevent supply shortages or overages. - Collaborate with clinical operations, quality assurance, and regulatory affairs to align supply plans with study milestones. - Prepare and maintain documentation for audits and inspections.

• Qualifications

  - Bachelor’s degree in Life Sciences, Supply Chain Management, or related field (Master’s preferred). - 5+ years of experience in clinical supply chain management or pharmaceutical operations. - Strong knowledge of GMP, GCP, and global regulatory requirements. - Proven ability to manage complex supply chains across multiple geographies. - Excellent organizational, analytical, and problem-solving skills. - Proficiency in supply chain management software and Microsoft Office Suite. - Strategic planning and execution - Vendor and stakeholder management - Regulatory compliance and quality focus - Adaptability in fast-paced environments - Strong communication and collaboration skills

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