Overview In this role you will draft, negotiate, and finalize complex clinical site contracts for sponsor-driven studies, ensuring timely execution and accurate data in CMS. You will partner with CBO, GCO, Legal, and site teams to manage contract lifecycles, budgets, and compliance in a fast-paced environment. You will drive timely deliverables, quality checks, and clear communication of issues and risks. This is a mission-driven opportunity to support cancer research through robust contracting and cross-functional collaboration. Responsabilidades * Draft, negotiate, and finalize clinical trial agreements and amendments with investigator sites * Manage contract budgets and ensure cost calculations align with protocol and site agreements * QC final contract and budget documents and initiate the signature process * Deliver final contracts within planned timelines while ensuring Fair Market Value compliance * Serve as primary liaison between CBO, Integral Clinical Operations, Legal,
sites and external providers * Track country/site intelligence and create contract process flows as needed * Forecast and communicate contract milestones; escalate risks to stakeholders * Collaborate on updates to contract templates and BeOne Medicines Legal Playbook * Maintain CMS records and real-time trackers; coordinate handoff to project/payment teams Requisitos principales * Knowledge of ICH-GCP and pharmaceutical regulations * Understanding of clinical trial contracting processes and clinical operations * Proven negotiation, interpersonal, and business skills * Strong planning, organizational abilities, and independent work capability * Fluency in English and local language; strong written/verbal communication * Ability to work in a fast-paced environment with tight deadlines * Travel up to 10% * Desirable: experience in financial, budget, cost management/analysis; IP, publication, and indemnification knowledge * negotiation * communication * proactivity * Microsoft Office * CTMS * Contract Lifecycle Management System