Study Coordinator

The Academic and Commercial Clinical Research Directorate at Vall d’Hebron Institute of Research supports clinical research teams at Vall d’Hebron University Hospital in commercial clinical trials. The Clinical Trials Management Unit oversees operational activities for these studies, ensuring adherence to protocols, Good Clinical Practice, and regulations. They seek a well-organized, methodical, people-oriented Study Coordinator for this unique role.

In daily work, coordinate patient recruitment, maintain clinical data in eCRFs, CTMS, and ISF, and perform data entry for Phase I-IV studies. Acquire pathology-specific knowledge for accurate protocol understanding and data extraction. Manage Investigational Medicinal Products accountability and support Adverse Events reporting.

Attend site monitoring visits, resolve queries per GCP, and coordinate sponsor equipment. Prepare documentation for audits or inspections and provide support to the clinical team. Report to the Clinical Trials Management Unit in a multidisciplinary environment at Vall d’Hebron Campus.

This position offers involvement across the Commercial and Contracted Clinical Research Directorate. Gain exposure to diverse clinical trial operations while supporting clinicians and Principal Investigators. Ideal for those motivated to contribute to high-quality clinical research.