As a Senior CRA, oversee clinical trial activities, ensuring compliance with protocols and regulations, and support site staff for successful trials.

Lead initiation of clinical trials, ensure compliance with regulations, and manage submissions and approvals for innovative treatments.

The Senior Clinical Research Associate oversees clinical trial activities, ensuring compliance with protocols and regulatory standards, while managing multiple sites and ensuring data integrity and participant safety.

As a Clinical Research Associate II, you will manage clinical trials, ensure compliance, analyze data, and support study documentation.

Oversees logistics operations for clinical trials, manages shipments and inventory, develops logistics strategies, collaborates with vendors, and ensures regulatory compliance.

As a Clinical Research Associate, you will conduct clinical trial visits, ensure protocol compliance, collaborate with site staff, and manage clinical data quality.

The Site Partner II coordinates site activations and maintenance, drives efficiency in clinical trials, and manages relationships with site teams and stakeholders.

The CRA monitors clinical trial sites for compliance with protocols, conducts site visits, trains site staff, and maintains relationships with stakeholders.