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Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; contribute to study documentation and clinical study reports.

Perform site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety. Collaborate with site staff, review data and resolve queries, and contribute to study documentation and clinical study reports.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; contribute to study documentation and clinical study reports.

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

Oversee clinical trial operations, manage cross-functional teams, ensure regulatory compliance, and handle budgets and timelines in early phase oncology studies.

Support feasibility activities for multiple clinical studies: manage CDAs, coordinate feasibility surveys, maintain site nomination trackers, liaise with sites/vendors, assist Feasibility Leads, and improve feasibility processes to ensure seamless study start-up.

The Clinical Trial Assistant will support clinical trials through administrative tasks, documentation management, and stakeholder communication to ensure smooth operations and compliance with regulations.