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The Lead CRA manages clinical trial sites, ensures compliance with regulations, mentors CRAs, and oversees data integrity. Responsibilities include site management, issue resolution, and collaboration with cross-functional teams.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring compliance and data integrity, while collaborating with site staff and preparing study documentation.

The Clinical Research Associate will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity, collaborating with study sites.

As a Clinical Research Associate, conduct site visits, ensure compliance and safety, collaborate with staff, and review clinical data documentation.

The Senior Clinical Research Associate will manage clinical trials, ensure compliance, analyze data, and collaborate with study personnel while traveling extensively.

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

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and study protocols, mentoring CRAs, and ensuring data integrity and patient safety.

Lead monitoring of clinical trials, ensuring adherence to protocols and standards. Conduct site visits, collaborate with teams, and train site staff. Build relationships for effective trial operations.

As a Senior Clinical Trial Manager, you will manage clinical trial operations, oversee budgets, develop monitoring plans, drive enrollment, and foster relationships with stakeholders.

The Clinical Systems Specialist will design and analyze clinical trials, interpret medical data, and support UAT processes within clinical systems.