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 problems of society and 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.Data Entry - Clinical Trials Management UnitThe Clinical Trials Management and Development Unit is responsible for following up on the execution of commercial clinical studies at the Vall d'Hebron Campus. The primary objective of this Unit is to contribute to the consolidation of the Vall d'Hebron University Hospital as an international clinical trial reference center, through the implementation of a new management model for clinical trials at Vall d'Hebron Campus. A management model that aims to ensure quality in clinical trials that generates opportunities for those researchers on campus, using the latest technology available to treat their patients and improve their quality of life.The number of clinical trials has increased in the last year at Vall d'Hebron University Hospital, not only in numbers but also in complexity, that helps patients and relatives to improve life expectancy. This requires well-organised, methodical, and people-oriented individuals who wish to develop their career in this field.The Clinical Trials Management Unit wants to incorporate to its team two (2) Data Entries who will be focused on clinical trials from different areas of knowledge.Job DescriptionEducation and QualificationsRequired:Bachelor's Degree in Health Sciences (preferable but not limited).Computer user level (Office package, mail).Fluency in Catalan and Spanish.Desired:Training in Good Clinical Practice (GCP) and clinical trials methodology.Experience and KnowledgeRequired:At least 2 years of experience working in a research environment.Knowledge of database programs.Ability to work independently as well as in a team environment.Good communication skills and fluency in written and spoken English.Desired:Experience with SAP management program.Organised and methodical person with high motivation and initiative.Able to give quick responses requested by the team and sponsor.Main Responsibilities and DutiesExtract data from the trial source documents.Complete and maintain up-to-date electronic case report forms (CRFs) and contribute to the resolution of queries.Manage the preparation and submission of images or results of medical procedures through the platforms provided by the sponsor.
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