The Academic and Commercial Clinical Research Directorate at Vall d’Hebron Institute of Research (VHIR) supports the clinical research community at Vall d’Hebron Campus throughout the entire lifecycle of commercial clinical trials. This Directorate assists clinical research teams at Vall d’Hebron University Hospital (HUVH) participating in clinical trials and provides support to companies interested in initiating clinical trials at HUVH.
As part of this directorate, the Clinical Trials Operations Unit is responsible for overseeing the operational activities of the clinical studies at the Vall d'Hebron Campus. The primary objective of this Unit is to support clinicians and Principal Investigators at Vall d’Hebron Campus in conducting their clinical studies in accordance with each study protocol, while adhering to Good Clinical Practice and current regulations.
We are currently looking for a well-organised, methodical,
and people-oriented individual to join the team as a unique role combining Study Coordinator with other general and specific responsibilities in the field of Clinical Research.
Main responsibilities and duties:
- Coordinate, manage, and promote patient recruitment for clinical trials.
- Maintain up-to-date clinical data from source documents to eCRFs, CTMS, and ISF.
- Perform data entry for phase I, II, III, and IV studies.
- Acquire pathology-specific knowledge to ensure accurate understanding of the protocol and data extraction from clinical source documents.
- 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 support to the clinical team and report t
📌 Study Coordinator (España)
🏢 VHIR
📍 España