Job Title:
Associate Director, Supply Chain

Company: Meet

Location: menlo, GA

Created: 2024-04-20

Job Type: Full Time

Job Description:

Associate Director, Clinical Supply ChainLocation: Menlo Park, CA (Hybrid, 3 days onsite)Responsibilities:The Associate Director, Clinical Supply Chain will play a pivotal role in overseeing the strategic planning and execution of clinical supply chain operations. Reporting to the Director of Supply Chain, this position will involve managing end-to-end supply chain activities to ensure the timely delivery of clinical trial materials while adhering to budgetary and regulatory requirements. Key responsibilities include:Leading a team of supply chain professionals to effectively manage clinical trial material logistics from planning through distribution.Collaborating closely with cross-functional teams including Clinical Operations, Manufacturing, Quality Assurance, and Regulatory Affairs to forecast demand, plan supply needs, and coordinate distribution activities.Developing and implementing supply chain strategies to optimize inventory management, minimize wastage, and reduce costs.Overseeing vendor relationships, including managing contracts, negotiating pricing, and evaluating vendor performance to ensure compliance with quality and regulatory standards.Driving continuous improvement initiatives to enhance operational efficiency, streamline processes, and mitigate supply chain risks.Qualifications:The ideal candidate will possess:A Bachelor's degree in Supply Chain Management, Operations Management, Business Administration, or a related field. An advanced degree is preferred.A minimum of 7 years of experience in clinical supply chain management within the pharmaceutical or biotechnology industry, with a proven track record of success in leading and managing supply chain operations.Strong leadership and project management skills, with the ability to effectively prioritize tasks, allocate resources, and drive results in a fast-paced environment.Proficiency in supply chain management software, IRT, and ERP systems, as well as a solid understanding of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP).Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal and external stakeholders at all levels of the organization.