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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.

Manage external budgets and contracts for clinical trials, ensuring alignment with regulations, and providing financial expertise to stakeholders.

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.

As a Clinical Trial Manager, you will lead global clinical trials, ensuring execution from startup to closeout while managing risks and collaborating with cross-functional teams.

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

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

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

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