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The Principal Manager, CQM leads document development and management, oversees compliance with procedures, and supports audits in clinical trials.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance, data integrity, and safety while collaborating with site staff.

The Clinical Research Associate will conduct site visits, ensure protocol compliance, manage data integrity, and collaborate with site staff in clinical trials.

As a Clinical Research Associate, you will conduct site visits for clinical trials, ensure compliance, and analyze clinical data. Collaborate with investigators, maintain data integrity, and contribute to study documentation.

Lead biostatistical components in clinical trials, oversee statistical activities, mentor junior statisticians, and ensure regulatory compliance.

The Senior Clinical Trial Manager will oversee clinical study budgets, develop monitoring plans, train Clinical Research Associates, and drive project enrollment, while managing relationships with stakeholders.

The Senior Clinical Research Associate will manage clinical trial activities, ensuring compliance with protocols and regulatory requirements while training site staff and maintaining data integrity.

Lead Clinical Research Associate will oversee and manage clinical trial sites, ensuring adherence to protocols and regulations while mentoring junior staff and ensuring data integrity.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and protocols while mentoring CRAs and collaborating with teams to execute trials effectively.

Manage and lead projects ensuring successful execution. Develop project plans, mentor teams, and collaborate with stakeholders to achieve goals.