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The Principal Clinical Data Science Lead will oversee data science methodologies in clinical research, manage teams, and ensure data insights support clinical development.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review data and resolve queries; contribute to study documentation and reporting.

The Clinical Research Associate manages clinical trial site activation by conducting site qualification visits, ensuring compliance with regulations, and collaborating with study teams and site staff to achieve study timelines.

Manage end-to-end contract lifecycle for clinical trial operations: draft, review, negotiate agreements, ensure regulatory compliance, advise project teams, monitor contract performance, and maintain contract records.