.Job Description:The Vall d'Hebron Research Institute (VHIR) is a public sector institution that promotes and develops research, innovation, and biosanitary teaching at the Vall d'Hebron University Hospital. Through the excellence of our research, we identify societal problems and contribute to spreading solutions worldwide.In April 2015, the Vall d'Hebron Research Institute (VHIR) obtained recognition from the European Commission in 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, nationality, religion, age, disability, or race.Position: Study Coordinator - Neurodegenerative Diseases Group The Neurodegenerative Diseases Group is focused on elucidating the molecular mechanisms of neuron cell death occurring in Parkinson's disease (PD) to develop new therapeutic strategies aimed at blocking neuronal dysfunction/degeneration in this currently incurable disease. The group performs clinical research, collaborating in the development of new drugs through participation in clinical trials phases I-IV.The Neurodegenerative Diseases Group at Vall d'Hebron Hospital seeks to incorporate a Clinical Trial Study Coordinator and Data Entry support for specific tasks.Education and Qualifications: Required: Bachelor Science degree (Biotechnology, Biology, Biochemistry, Pharmacy, Nursing, or other science bachelor degree).Training in good clinical practice and clinical trials methodology is desired.Good communication skills and fluency in written and spoken English.Computer user level (Office package, email).Organized and methodical person with high motivation and initiative.Quick response to time requests by the team and sponsor.Experience and Knowledge: Experience with SAP management program (not mandatory).Ability to work independently as well as in a team environment.Main Responsibilities and Duties: Data entry for phases I, II, III, and IV clinical trials and project research in Neurodegenerative Diseases.Keep up-to-date clinical data from source documents into the CRFs.Answer queries and provide quick feedback to sponsor and clinical team.Support the clinical team and the Clinical Trial Coordination Unit.Ensure maximum adherence to the protocol and avoid deviations.Assist the research team in the tasks necessary for the development of studies.Attend site monitoring visits, review, and resolve queries in accordance with GCP.Labour Conditions: Full-time/Part-time position: 40h/week, but might be extended to more hours on database lock days.Starting date: immediate.Possibility to work some days remotely