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 general 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
Global 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 (San Sebastián)
🏢 Syneos Health
📍 San Sebastián