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The Clinical Data Reviewer is responsible for clinical data assessment, checking data validity, generating queries, and supporting clinical trials for oncology drug development, ensuring data quality for submissions and analyses.

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 Sr. Site Contracts Specialist leads contract negotiation and management for clinical trials, ensuring compliance and fostering collaboration with stakeholders. Responsibilities include preparing contracts, managing budgets, and training junior staff, while maintaining project timelines and quality standards.

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.

Oversee clinical trial operations focusing on patient safety, data integrity, and compliance while leading site management and team collaboration.

The role involves programming and data review for real-world data analysis, supporting epidemiologists, and managing complex data sets using statistical programming languages and tools.

The Clinical Trial Manager II oversees clinical trials, ensuring compliance with regulations, managing site interactions, and coordinating teams to meet project milestones.

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

The Associate Director of Epidemiology RWE provides operational and technical support for RWE studies, ensuring timely task execution and documentation accuracy.