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, General 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