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The Senior Clinical Trial Manager oversees clinical budgets, develops monitoring plans, drives enrollment, optimizes CRA performance, and maintains study integrity. They also manage relationships with stakeholders and mentor team members.

The Clinical Study Specialist organizes reports, schedules meetings, reviews study documents, tracks site activities, and supports clinical trials.

As a Clinical Research Associate, you will conduct clinical trial visits, ensure protocol compliance, and collaborate with site staff while maintaining data integrity and patient safety.

The Project Manager will drive and accelerate the activation of clinical sites, ensuring timely and quality delivery while coordinating with stakeholders and managing project activities.

Oversee site contracts for clinical studies, manage contract development, collaborate with teams, ensure financial management, and mentor others.

As a Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements, managing sites, and supporting data integrity and participant safety.

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

The Clinical Research Associate will conduct clinical trial visits, ensure protocol compliance, analyze data, and prepare study documentation while collaborating with site staff.

Oversee and manage clinical trial activities, ensuring adherence to protocols, regulatory requirements, data integrity, and participant safety. Conduct site visits, provide support, and maintain relationships with stakeholders.

The Clinical Research Associate will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity during studies.