Overview In this role you will guide late-phase Hematology/Immunology trials as a sponsor-side Clinical Project Manager II. You’ll coordinate with CROs and vendors, drive study timelines, and oversee documentation and risk management. You’ll partner with cross-functional teams to ensure trial deliverables meet SOP, GCP, and regulatory standards. This position offers global scope and a chance to shape pivotal studies within a mission-driven organization. Responsabilidades * Support the Clinical Trial Manager/operational team in trial execution * Liaise with CROs and ancillary vendors to manage trial tasks * Maintain effective communication with the project team and provide status reports to align with timelines * Review, develop, and write clinical trial documents and manuals (study manuals, biomarker plans)



and create Master ICF template * Review and approve site changes in consultation with legal and safety when warranted; update templates for risks and amendments information Requisitos principales * Prior sponsor-side experience * General study experience * Oncology, Hematology, or Immunology therapeutic area expertise, ideally with complex/pivotal studies * End-to-end study management experience * Strong communication skills in a fast-paced environment * Proactive ownership * Strong communication and collaboration with internal teams, sites, and vendors * Strong prioritization and organizational skills * Clinical trial documentation development * Master ICF template creation * Site and vendor coordination

📌 Single Sponsor Clinical Project Manager II (Santiago de Compostela)
🏢 Syneos Health
📍 Santiago de Compostela