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The Principal Biostatistician leads RWD studies, mentoring biostatisticians, preparing statistical plans, reviewing data, and ensuring high-quality project completion. Requires RWD experience and a PhD.

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

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

The Sr. Project Specialist manages project files and financial reports, leads meetings, records KPIs, supports audits, and may mentor junior staff.

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.

The Site Activation Specialist manages site activation processes for clinical trials, ensuring timely submissions and compliance with regulatory standards, while supporting project budgets and quality deliverables.