Are you an experienced Study Coordinator with a background in oncology and hematology clinical trials ? We are looking for a motivated and detail-oriented professional to support an ongoing clinical research project in the Valencia region . About the Role As a Study Coordinator, you will provide onsite support to the study team for approximately one day per week over a period of around three months , with a primary focus on data entry and site coordination activities . This is an excellent opportunity for someone seeking a flexible, part-time role while remaining actively involved in clinical research. Key Responsibilities Perform timely and accurate data entry in the electronic data capture (EDC) system. Review source documents and ensure data completeness and consistency. Resolve data queries in collaboration with investigators, monitors, and site staff. Support study documentation and maintenance of the Investigator Site File (ISF). Collaborate closely with the clinical research tea...