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You will be updated with latest job alerts via emailThe Paediatric Hepatology and Liver Transplantation Unit at Vall dHebron Hospital manages approximately 300 new cases of rare paediatric liver diseases annually and performs around 25 paediatric liver transplants each year. The unit is officially designated as a national reference centre (CSUR) for both Paediatric Liver Transplantation and Complex Paediatric Hepatic Disorders.
We offer access to state-of-the-art hepatic surgery and world-class interventional radiology enabling advanced multidisciplinary care across a wide range of complex conditions including metabolic genetic autoimmune and vascular liver diseases. Our comprehensive services include the full continuum of care: from diagnostics and acute management to long-term follow-up post-transplant.
Research is conducted through the Hepato-bilio-pancreatic surgery (HBP) and liver transplantation Research Group at VHIR currently coordinating or participating in approximately 15 clinical trials and over 40 internal and collaborative research projects including national and international registries.
The selected candidate will join a highly active and collaborative team contributing to the development and implementation of clinical studies patient registries and translational research in the field of paediatric hepatology and transplantation.
Education and qualifications:
University Degree in Health Science preferred.
High academic records.
Excellent written and oral communication in Catalan Spanish and English.
At least 1 year of experience working in hospital environments
Experience with SAP management software
Moderate to high knowledge of statistics
Previous Knowledge in Networks
High motivation for a research career.
Ability to work in a team and the responsibility and ability to achieve commitment to the word.
Main responsibilities and duties:
Manage Investigational Medicinal Product returned from patients and keep related accountability and adherence information up to date.
Support the notification process of Adverse Events and Serious Adverse Events.
Attend site monitoring visits review and resolve queries in accordance with GCP.
Coordinate the reception and return of equipment provided by the sponsor.
Prepare required documentation in case of audit or inspection visits.
Provide oversight of intern training and mentorship.
Provide support to the clinical team and report to the Clinical Trials Management Unit.
Provide support for all tasks related to the Commercial and Contracted Clinical Research Directorate as assigned by the Manager.
Labour conditions:
Deadline to apply:
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 gender identity and expression religion age functional diversity or ethnicity.
Full Time