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Manage negotiation and execution of clinical study agreements (CTAs) while ensuring compliance with sponsor and company requirements. Build strong relationships with stakeholders and support operational initiatives for site contracting and budgeting goals.

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

The Clinical Data Reviewer will work in the oncology field, ensuring data integrity for clinical trials and collaborating with teams to meet customer needs.

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

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

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.