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 integral 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 (Global experience needed) Fully home based in Spain, Bul (León)
🏢 Syneos Health
📍 León