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The Scientific Affairs Specialist I supports scientific liaison activities for central laboratory services in clinical trials, ensuring scientific rigor and compliance. Responsibilities include managing test information, supporting assay selection, and collaborating with cross-functional teams.

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

The Senior Clinical Research Associate will manage clinical trials by conducting site visits, ensuring compliance, and contributing to study documentation.

The Clinical Research Associate will conduct site visits, ensure protocol compliance, and review clinical data for trials. Responsibilities include collaborating with investigators and preparing study documentation.

As a Clinical Research Associate, you'll conduct clinical trial visits, ensure protocol compliance, manage data quality, and assist in study documentation.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

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

The Principal Biostatistician leads Phase I-III clinical trials, overseeing statistical activities and mentoring junior statisticians while engaging with clients and regulatory agencies.