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The Senior Clinical Research Associate will oversee clinical trials, ensuring compliance, maintaining data integrity, and preparing study documentation while collaborating with investigators and site staff.

The Contract Specialist coordinates, prepares, and executes clinical study contracts, ensuring compliance with GCP/ICH regulations and collaborating with project teams.

The Senior Clinical Research Associate will oversee clinical trial activities, ensuring adherence to protocols, conduct site visits, and manage data integrity while providing support and training to site staff.

The Senior CRA ensures quality execution at clinical trial sites, conducts oversight visits, supports compliance, and enhances quality performance across studies.

Oversee and manage clinical trial activities, ensuring adherence to protocols and regulatory requirements, while maintaining data integrity and participant safety.

As a Senior CRA / CRA II, you will manage and oversee clinical trial activities, ensuring compliance with protocols, regulations, and industry standards through monitoring and site visits.

As a Clinical Trial Assistant, you'll provide administrative support for clinical trials, manage documentation, assist in regulatory submissions, and collaborate with cross-functional teams to ensure trial success.

Lead and manage complex programs, coordinating teams and resources to ensure timely delivery within budget, while driving process improvements and strategic initiatives.

The Digital Media Buyer develops and implements digital advertising campaigns for patient recruitment, optimizing performance and collaborating on content creation.

The Trial Project Manager leads clinical studies, ensuring timelines, quality, and recruitment goals are met while promoting operational excellence and cross-functional collaboration.