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The Senior CTA will manage clinical trial site activities, ensure compliance with protocols, assist in regulatory document preparation, and mentor junior staff.

The Manager, Site Resourcing will oversee site management for clinical research, coordinate teams and budget, and ensure compliance with regulations.

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 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 Clinical Research Associate will conduct monitoring visits for clinical trials, ensuring compliance and data integrity, and preparing study documentation.

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

The Clinical Research Associate will conduct site visits, ensure compliance and patient safety, and review clinical data with a focus on trial operations.

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

Lead one or more Clinical Data Science project teams, oversee project initiation, planning, and execution, and manage communication with clients and vendors. Four key responsibilities include quality control, issue tracking, project kick-off facilitation, and support in sales efforts.