Experteer 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.

Compensaciones / Ventajas
• 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, Global 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

Responsabilidades
• 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

Requisitos principales
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📌 Senior Contract Associate, Clinical Site Contracts (España)
🏢 Beigene
📍 España