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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 Statistical Programmer develops programming code using SAS to generate datasets, summary tables, and graphs, while ensuring quality and compliance with standards, manages project documentation, and mentors junior staff.

The Clinical Scientist contributes to protocol design, scale management, and provides training on clinical scales while ensuring data consistency and performing statistical analysis.

The Site Activation Specialist II/Sr. will manage site start-up activities, including regulatory submissions, contract negotiations, and site communication to ensure efficient clinical trial initiation and compliance with quality standards.

Oversee clinical trial management, site interactions, and compliance. Collaborate across teams to meet study milestones and manage risks. Train study staff and maintain project oversight and quality.

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.