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Negotiate, draft, review, and finalize clinical trial agreements, amendments, and ancillary documents with study sites. Maintain stakeholder communication, track contract progress in ICON/client systems, identify risks, support site start-up, file contractual documents, and participate in study team calls while adhering to SOPs and training requirements.

The Oncology Project Manager will lead clinical trial projects, manage global teams, ensure project execution, and coordinate training and stakeholder communication.

The Manager, Production Operations oversees day-to-day production activities, ensuring efficiency, quality standards, and alignment with organizational goals while leading a team and collaborating across departments for process optimization.

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

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

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; contribute to study documentation and clinical study reports.

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.

The Feasibility Principal Analyst leads feasibility strategy and analysis for clinical studies, synthesizing data to inform study planning and enrollment decisions while mentoring junior team members.

The Senior Biostatistician II will oversee clinical trials, manage statistical deliverables, lead client interactions, and mentor junior staff.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with sites; review data and support study documentation.