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The intern will assist the QMS team in document review, authorship, compliance, and change control activities, ensuring document clarity and adherence to guidelines.

The GCO Program Lead is responsible for strategic operational planning, program management, and leading clinical operations teams to ensure excellence in clinical trials. This role involves mentorship, resource management, and collaboration with cross-functional teams.

The Regional Business Manager will analyze market dynamics, drive sales strategies, lead training initiatives, and enhance leadership within the region to achieve business goals.

As a Data Insights Intern, you will manage and transform data from clinical trials to support quality management, develop systems for data use, and generate insights for decision-making.

Lead Global Clinical Operations compliance activities, ensuring ICH GCP and regulatory adherence. Develop risk management, root cause analysis, CAPA, inspection preparedness, and quality-by-design for clinical studies. Partner with cross-functional stakeholders to embed preventive compliance, monitor trends, escalate significant issues, and report compliance status to leadership.

The Senior Learning Business Partner in Global Clinical Operations focuses on developing technical and leadership capabilities, designing training programs, and ensuring alignment with regulatory standards.

The Director, Global Regulatory Project Management leads oncology regulatory strategies, ensuring successful global drug submissions, while driving operational excellence and collaboration across teams.

The Associate Director is responsible for leading global regulatory project management, ensuring successful regulatory submissions, and facilitating cross-functional collaboration to maintain product market access worldwide.

Lead the Central Statistical Monitoring team, ensuring subject safety and data integrity in clinical trials through statistical analysis and collaboration with various stakeholders.

The Director of Global Regulatory Project Management leads oncology regulatory strategies, ensures timely submissions, manages global project teams, and fosters cross-regional collaboration to maintain market access for products.