Top Tech Jobs & Startup Jobs in Charlotte, NC

The Manager designs and implements learning solutions for global clinical operations teams, collaborating with stakeholders to enhance training content and effectiveness while ensuring compliance with regulations.

The Director will manage global regulatory strategies and processes, provide leadership on regulatory issues, and interface with business partners and regulatory authorities to secure product approvals and market access.

The role requires leading drug development and project management for the Biotech Unit, including strategy development, team management, and cross-functional collaboration within a global context.

The Director, Global R&D Compliance will lead compliance guidance for R&D functions, ensuring adherence to regulatory standards, and developing effective policies and training. This role requires strategic advisory skills and collaboration with various stakeholders.

Support implementation of the Culture of Quality program, enhance Quality communications (webpage, newsletters, sessions), create a Quality department storyboard, produce graphic and digital content, collect and analyze data, and collaborate cross-functionally to advance quality initiatives.

The Associate Director will drive digital tool adoption, develop communication strategies, train users, monitor progress, and oversee AI capabilities in Quality processes.

Lead global strategic feasibility for clinical studies by integrating internal and external data, advising country/site selection, recruitment and operational strategies, improving feasibility processes and tools, and partnering with program and study teams to optimize study design and execution across early to late-stage programs.

Lead the U.S. Biologics Regulatory CMC organization, develop global CMC regulatory strategies, oversee CMC submissions and health authority interactions, manage a ~15-person team, ensure compliance and inspection readiness, and support lifecycle management for biologics including mAbs, ADCs, cell therapies, and combination products.

The Executive Director leads Global Clinical Pharmacology & Development Technology Solutions, overseeing technology strategy, solution delivery, and team leadership to support R&D initiatives in cancer treatment.

The Sr Manager of Clinical Supply Chain oversees drug supply activities, manages relationships with stakeholders, ensures supply continuity, and leads process improvements.