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As a Senior Clinical Research Associate, you will oversee clinical trials, ensuring adherence to protocols and regulatory standards, managing multiple sites, and collaborating with teams for data integrity and compliance.

As a Clinical Research Associate, you will conduct and monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff and investigators.

The Study Start-Up Manager oversees study planning and activation deliverables, ensuring compliance with regulations and managing SSU activities across assigned projects.

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

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

The Principal Biostatistician leads Phase I-III clinical trials, overseeing statistical activities and mentoring junior statisticians while engaging with clients and regulatory agencies.