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.

ResponsabilidadesSupport the Clinical Trial Manager/operational team in trial executionLiaise with CROs and ancillary vendors to manage trial tasksMaintain effective communication with the project team and provide status reports to align with timelinesReview, develop, and write clinical trial documents and manuals (study manuals, biomarker plans)



and create Master ICF templateReview and approve site changes in consultation with legal and safety when warranted; update templates for risks and amendments information Requisitos principalesPrior sponsor-side experienceGlobal study experienceOncology, Hematology, or Immunology therapeutic area expertise, ideally with complex/pivotal studiesEnd-to-end study management experienceStrong communication skills in a fast-paced environmentProactive ownershipStrong communication and collaboration with internal teams, sites, and vendorsStrong prioritization and organizational skillsClinical trial documentation developmentMaster ICF template creationSite and vendor coordination

📌 Single Sponsor Clinical Project Manager II (Global experience needed) Fully home based in Spain, Bul (Madrid)
🏢 Jobrapido
📍 Madrid