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, VHIR obtained the recognition of the European Commission HR Excellence.
This recognition proves that VHIR endorses the 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 - Neurovascular Diseases GroupVHIR offers a vacant position for a Study Coordinator to work on the project "A multicenter, prospective, non-interventional study to determine the cut-off and clinical performance of the Elecsys Amyloid Plasma Panel and its component assays."
Job DescriptionEducation and QualificationsRequired: Bachelor's Degree in PsychologyMaster in NeuropsychologyExperience and KnowledgeRequired: Previous experience in clinical trials coordination.Training in good clinical practice and clinical trials methodology is desired.Good communication skills and high fluency in written and spoken English.Personal skills: well-organized, methodical, proactive, and aptitude for teamwork.Desired: Experience in Alzheimer's Disease (or other neurodegenerative diseases) clinical trials.Previous experience as a psychometric rater in clinical trials.Experience with SAP management program (not mandatory).Main Responsibilities and DutiesData entry in the context of this project.Keep up-to-date clinical data from source documents into the CRFs.Answer queries and give quick feedback to sponsor and clinical team.Support the clinical team and assist the research team in tasks necessary for the development of studies, ensuring maximum adherence to the protocol.Attend site monitoring visits, review, and resolve queries in accordance with GCP.Labour ConditionsPart-time position: 20h/week.Starting date: Immediate.Gross annual salary: 12,000 euros.Contract: Permanent linked to a project.
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