Study Coordinator - Phase I Oncology Clinical Trials

Description

**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 aim to attract top professional talent to continue offering differentiated healthcare services distinguished by quality, high specialization, and person-to-person 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 58 hospitals. Our network of centers features the most advanced technology and a highly specialized, internationally recognized team. At Quirónsalud, we are dedicated to improving the health and well-being of both our patients and our professionals. From Quirónsalud’s private hospitals in Madrid, we are seeking a **Study Coordinator for Hospital Universitario Quirónsalud Pozuelo**, located in Pozuelo de Alarcón. What will be your **mission**? Coordinate with the Principal Investigator and institution to ensure that Phase I Oncology clinical trials and related activities comply with current national regulations and sponsor policies and procedures. What will be your **main functions and responsibilities**? * Coordinate tasks related to clinical trials within the Oncology Department. * Ensure coordination and communication between the sponsor and the research team, as well as with all other personnel involved in clinical trials. * Maintain and manage documentation related to clinical trials within the Medical Oncology Department. * Schedule patient visits. * Support nursing staff in maintaining associated consumable materials and managing their stock control. * Complete information in the Case Report Form (CRF). Enter data, maintain, report, and follow up on serious adverse events, resolving queries generated in the CRF as promptly as possible. * Contact the sponsor-designated personnel periodically to keep patient and visit information updated. Host monitoring visits. * Manage and dispatch biological samples to local and central laboratories. * Serve as the local point of contact for reporting patient adverse events within the stipulated timeframe. * Support nursing staff in Phase I oncology clinical trials. * Other duties related to the position. What do we offer and what are our benefits? * Immediate incorporation into a collaborative and specialized team (September). * Weekly working hours: 37\.5h. * **Working schedule: Monday to Thursday, 8:00\-14:00 and 14:30\-16:30; Friday, 8:00\-13:30.** * **Indefinite-term contract.** * Internal mobility and promotion policy. * Attractive, competitive, and market-aligned remuneration package. * Flexible compensation for childcare, transportation, health insurance, and meals. * Strategic training plan enabling 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 well-being programs and access to the Digital Hospital. + Family wellness: initiatives promoting healthy lifestyles and work-life balance. **If you seek a professional career in a prestigious, innovative hospital environment with development opportunities within an organization committed to the health of its patients and professionals, we invite you to join our team!** *At Quirónsalud, we promote integration and respect for diversity. Therefore, our selection processes are conducted under these principles. Likewise, the company declares its commitment to establishing and developing practices that foster and encourage equal treatment and opportunities between men and women, without direct or indirect discrimination based on gender. This principle forms part of our Corporate and People Policy, aligned with Organic Law 3/2007, of March 22, on Effective Equality between Women and Men.* **Requirements** -------------- * English level B2 (minimum). * Training, knowledge, and experience in clinical trials will be valued. * A master’s degree or specialized training in clinical trials is highly desirable. * Nursing or equivalent training will be especially valued. * Scientific knowledge. * Ability to work effectively in a team. * Autonomous, responsible, proactive, and initiative-driven individual. Do you already have a profile on ? Autocomplete with b4work **Location:** Madrid (Spain)**Vacancies:** 1**Work mode:** On-site