Descripción de la oferta
Clinical Research Coordinator – Toledo (Part-Time, 20-24hours/week)Start Date : immediatelyDuration : until 30th of September 2026Antes de solicitar este puesto, por favor, lea la siguiente información sobre esta oportunidad que encontrará a continuación.IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Toledo. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.Key ResponsibilitiesAs a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:- Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems- Supporting patient screening and enrollment, including handling informed consent and privacy documentation- Coordinating logistical activities for study procedures in line with the study protocol- Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness- Managing and shipping biological samples- Communicating with study monitors and responding to study-related inquiries- Help with patient recruitment, patient education and community outreach- Carrying out general administrative tasks related to the studyYour ProfileWe are looking for candidates who bring a combination of education, experience, and skills:- Bachelor's degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.G., clinical research coordinator, research assistant, nurse, medical assistant)- Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules- good knowledge of medical terminology- Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)- Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site- Excellent interpersonal and communication skills- Strong organizational skills and attention to detail- Fluency in Spanish and good command of EnglishWhy Join IQVIA?At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.Interested? xqysrnhIf this sounds like the right opportunity for you, we encourage you to apply today.
