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Job Summary: Coordinate hematology clinical trials, ensuring regulatory compliance and effective communication between the sponsor and the research team, as well as managing documentation and patient visits. Key Responsibilities: 1. Coordination of clinical trials in Hematology. 2. Management of documentation and communication with research teams. 3. Planning of patient visits and data follow-up. **Quirónsalud** --------------- Quirónsalud is the leading healthcare services provider in Spain. We have internationally renowned experts in the biomedical field and a large team of healthcare and non-healthcare professionals who work daily to deliver the highest quality specialized care in our country. At Quirónsalud, we seek top professional talent to continue offering differentiated healthcare services distinguished by quality, high specialization, and person-centered health care. **Job Description** ---------------------------- **Quirónsalud** is the leading healthcare group in Spain and, together with its parent company Fresenius\-Helios, also in Europe. We have a team of over 50,000 professionals distributed across more than 180 healthcare centers, including 57 hospitals. Our network of centers features the most advanced technology and a highly specialized, internationally renowned team. At Quirónsalud, we are dedicated to improving the health and wellbeing of our patients—and also of our professionals. From Quirónsalud’s private hospitals in Madrid, we are seeking a **Study Coordinator for Hematology Clinical Trials** at the **Quirónsalud University Hospital Madrid, located in Pozuelo de Alarcón.** What will be your **mission**? Collaborate with the Principal Investigator and institution to ensure that clinical trials and related activities are conducted in accordance with current national regulations. What will be your **main duties and responsibilities**? * Coordinate tasks related to clinical trials within the Hematology Department. * Ensure coordination and communication between the sponsor and the research team, as well as with all other personnel involved in the clinical trials. * Maintain and manage documentation related to clinical trials in the Hematology Department. * Plan patient visits. * Complete information in the case report form (CRF). * Periodically contact the personnel designated by the study sponsor to keep patient and visit information up to date. Host monitoring visits. * Manage and ship biological samples to local and central laboratories. * Serve as the local point of contact for reporting and managing patient adverse events within the established timeframe. What do we offer and what are our benefits? * Immediate hiring * Permanent contract * Full-time position * **Working hours: 8:00–17:00 Monday–Thursday (split shift), and 8:00–15:00 on Friday** * Internal mobility and promotion policy * Flexible compensation for daycare, transportation, health insurance, and meals * Strategic training plan enabling both personal and professional development * Access to the Quirónsalud Contigo program: * Financial wellness: access to the Payflow platform and exclusive discounts. * Health wellness: physical and mental wellbeing programs and access to the Digital Hospital. * Family wellness: initiatives focused on promoting healthy lifestyles and work-life balance. We look forward to welcoming you! **Requirements** -------------- Do you meet the following **requirements**? * University diploma or degree * Clinical trials training or master’s degree is highly desirable * Prior experience managing clinical trials/studies in Hematology/Oncology or other medical specialties is valued * Advanced English proficiency (C1\) is desirable Do you already have a profile on ? Autocomplete with b4work **Location:** Pozuelo de Alarcón (Spain)**Contract Type:** Permanent**Working Hours:** Full-time**Vacancies:** 1**Discipline:** Others**Work Modality:** On-site
