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 (Global experience needed) Fully home based in Spain, Bulgaria, Poland or UK. (Murcia)
🏢 Syneos Health
📍 Murcia