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 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 - Clinical Trials Management Unit The Clinical Trials Management and Development Unit is responsible for following up 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 centre, 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, helping 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 a Study Coordinator who will be focused on Hepatocellular Carcinoma clinical trials.
Job Description Education and Qualifications Required: Bachelor's Degree in Health Sciences (preferable but not limited).
Computer user level (Office package, mail).
Fluency in Catalan and Spanish.
Desired: Master in Clinical Trial Management (CTM) or similar training program.
Training in Good Clinical Practice (GCP) and clinical trials methodology.
Experience and Knowledge Required: At least 2 years of experience working in a hospital environment and research.
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.
Quick response to time requested by the team and sponsor.
Main Responsibilities and Duties Coordinate/manage and promote patient recruitment for clinical trials.
Run data entry for Phase I, II, III, and IV studies.
Keep up-to-date clinical data from source documents to eCRFs.
Keep up-to-date Clinical Trial Management System (CTMS).
Answer queries and provide quick feedback to sponsor and clinical team.
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