Clinical Drug Supply & Trial Manager

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.About the Role: Responsible for developing drug supply planning strategy and overall management of supplies for late phase clinical studies. Additionally, for assigned early phase trials, supporting the overall management of assigned clinical studies including project planning, timelines, clinical budgets, resource management, vendor selection/management, and key project deliverables. Key Responsibilities Responsible for developing drug supply planning strategy and overall management of supplies for late phase clinical studies Manage clinical supply planning and create drug supply forecast for packaging and labeling operations for study protocols. Interpret relevant protocol information to develop packaging/labeling design and/or global distribution strategy (e.g., location of depots) Coordinate the origination, proofing and translation of clinical study labels, as required Support design and set-up and provide oversight of specifications for clinical IRT/IVRS system (automated randomization/drug supply management system) Oversee a variety of logistics issues, including but are not limited to supply chain services, inventory control, import-export, shipment of products and third-party warehousing Maintain close communications with all internal-chain groups to ensure the adequate supply of clinical supplies throughout the duration of a clinical trial Provide oversight of clinical drug supplies per vendor oversight plans Coordinate and manage drug supply vendors including regular meetings with vendor and clinical operations, ensuring meeting documentation is maintained for the study TMFs, as applicable Track clinical supply expiration, and taking into account drug supply forecasts/ enrollment/ inventory levels, ensure new drug manufacturing, packaging, labeling are initiated with adequate time to re-supply clinical study sites as required Select and manage vendors, including CRO organizations, ac...