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The Clinical Project Manager II will oversee biomarker study operations, manage cross-functional teams, and ensure high-quality project delivery throughout clinical trials.

Manage biomarker study operations, coordinate cross-functional teams, oversee specimen collection and analysis, and ensure project delivery in clinical trials.

The Principal Research Scientist will develop, validate, and optimize bioanalytical methods, drive innovation, supervise staff, and ensure compliance with standards.

The Sr Clinical Research Associate performs site management, monitoring, regulatory compliance, and training while ensuring patient safety and data integrity throughout clinical trials.

The Site Contracts Lead will collaborate globally with customers in drug development, ensure compliance, and facilitate contract negotiations.

Manage global site activation efforts, ensuring timely delivery of key milestones while collaborating with sponsors and cross-functional teams in clinical operations.

The Director of Epidemiology Pipeline collaborates on virology clinical trials, providing scientific expertise, leading project proposals, and overseeing study management and regulatory compliance.

The Senior Clinical Project Manager will lead Phase III oncology and hematology trials, managing projects and cross-functional teams while ensuring timely and quality delivery.

The Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.

Responsible for monitoring clinical trial sites, ensuring compliance with regulatory standards, managing site activities, and supporting patient recruitment throughout study lifecycle.