.Detalles del empleoTipo de empleo: Jornada completaUbicación: Barcelona, Barcelona provinciaDescripción completa del empleo:The Vall d'Hebron Research Institute (VHIR) is a public sector institution that promotes and develops the research, innovation and biosanitary teaching of the Vall d'Hebron University Hospital. Through the excellence of our research, we identify and apply new solutions to the health problems of society and we contribute to spread them around the world.In April 2015, the Vall d'Hebron Research Institute (VHIR) obtained the recognition of the European Commission HR Excellence. This recognition proves that VHIR endorses the general principles of the European Charter for Researchers and a Code of Conduct for the Recruitment of Researchers (Charter & Code). VHIR embraces Equality and Diversity. As reflected in our values, we work toward ensuring inclusion and equal opportunity in recruitment, hiring, training, and management for all staff within the organization, regardless of gender, civil status, family status, sexual orientation, religion, age, disability or race.Study Coordinator / Data Manager Infectious Diseases GroupThe Infectious Diseases Group is a multidisciplinary research team that collaborates in the development of new treatments for different infections through participation in clinical trials and basic research projects to improve the quality of life of patients with any infection.We offer a vacant position for a data manager and study coordinator of the clinical research projects within the Infectious Diseases group.Job Description Education and qualifications:Required:Degree in Life or Health Sciences (Biology, Biomedicine, Biochemistry, Pharmacy)Desired:Knowledge in Clinical Trial MonitoringExperience and knowledge:Required:Ability to work in a multidisciplinary teamMotivation for clinical researchEnglish: fluent written and spoken (B2 or above ideal)A good computer literacy level; basic MS officeDesired:Training and experience in clinical trials and clinical researchKnowledge of the specific legislation for clinical trials and clinical research will be positively valued.Experience in Research Institutions and/or in Project Management within biotech and/or scientific environments will be positively valuedKnowledge of compliance and data protection legislation (LOPD, GDPR).Knowledge and experience on statistics and software (R, python, SQL, etc) will be positively valuedMethodical and well-organizedHigh motivation and initiativeGood communication skillsMain responsibilities and duties:Coordinating and handling all activities regarding clinical trials and research projects related to HIV/STI, COVID and other infectious diseases