ppIn this role you will draft, negotiate, and finalize complex clinical site contracts for sponsor-driven trials, ensuring timely data entry and adherence to timelines. You will act as the main liaison between CBO, GCO, Legal, sites, and vendors to manage contracting lifecycles. The position demands fast-paced execution with strong prioritization and issue communication. Your work supports compliant, value-aligned agreements that enable trial progress and site partnerships. This is a mission-driven opportunity to help advance cancer research through efficient contracting and cross-functional collaboration. /pulliPrepare, negotiate, and finalize clinical trial agreements and amendments with sites /liliManage contract budgets and ensure cost calculations align with protocol and site agreements /liliQC final contracts and budgets and initiate signature processes /liliDeliver contracts within timelines and ensure FMV compliance /liliServe as primary contact between CBO, GCO, Legal, sites,



and external providers /liliMaintain country/site intelligence and tailor contract processes accordingly /liliForecast and track fully executed contract dates and communicate risks /liliUpdate contract templates with CM and BeiGene Legal; contribute to Legal Playbook updates /liliCoordinate with IPM to ensure site contracts are approved and executed per policies /liliEnsure legal/DM approvals precede execution and translate contracts as needed /liliMaintain ongoing communication with site personnel and internal partners throughout lifecycle /liliPrepare amendments, notes to file, and related documents /liliEscalate issues and delays to stakeholders as needed /liliParticipate in investigator site and project meetings and maintain CMS records /liliHandoff to project/payment team after execution of final documents /liliClinical trial contracting and budgeting experience in pharma/CRO/vendor (3+ years) /liliStrong negotiation, interpersonal and business skills /liliKnowledge of ICH‑GCP and regulatory guidelines /liliUnderstanding of clinical contracting processes and operational practices /liliExperience with financial planning, budget management, and fair market value concepts /liliAbility to work independently in a fast-paced, deadline‑driven environment /liliExcellent written and verbal communication in English (and local language where applicable) /liliProactive, team-oriented, and capable of handling ambiguity and change /li /ulpIn this role you will draft, negotiate, and finalize complex clinical site contracts for sponsor-driven trials, ensuring timely data entry a… /p /p #J-18808-Ljbffr

📌 Senior Contract Associate (Italia)
🏢 Experteer Italy
📍 Italia