T4 PT ISCIII 23
Call for a T4 PT ISCIII 23 the UICEC. Deadline: 3 July 2026, 15:00 h.
About the Unit / Group
The Sant Pau UICEC provides comprehensive support to researchers in the development of independent research projects promoted by the Sant Pau Research Institute (and not sponsored by the pharmaceutical industry), covering methodological, regulatory, administrative, financial, and operational aspects, while ensuring compliance with ethical standards, applicable legislation, and Good Clinical Practice guidelines.
The Sant Pau UICEC is part of the Spanish Clinical Research Network, an organization that supports the development of independent multicenter clinical trials, and belongs to the SCReN platform (Spanish Clinical Research Network ISCIII).
Essential requirements
- Minimum qualification required: University Degree (Bachelor's, Engineering, Architecture); Graduates with ≥300 ECTS corresponding to Level 3 (Master's Degree); Graduates holding a Master's Degree in Clinical Trials (≥300 ECTS). Technical Engineers, Technical Architects, and Diploma holders with a Level 3 Master's Degree.
- Oral and written proficiency in both official languages of Catalonia or, alternatively, the selected candidate must demonstrate or commit to acquiring adequate proficiency in both languages within a maximum period of one year.
- Advanced level of English.
- Advanced proficiency in office software tools (Excel, Word, PowerPoint, etc.).
- ICH E6 (R3) training certificate. Skills will be valued
- Professional experience in Research Institutes affiliated with hospitals.
- Experience in monitoring independent/academic clinical trials.
- Experience as a Clinical Trial Assistant.
- Experience as a Clinical Trial Coordinator in hospital settings.
Functions
- Plan and conduct site selection, initiation, routine monitoring, and close-out visits, preparing the corresponding reports and following up on pending actions, ensuring compliance with the protocol, Good Clinical Practice Guidelines (ICH- GCP E6 (R3)), and applicable regulations (Royal Decree 1090/2015 and Regulation (EU) No. 536/2014).
- Verify compliance with the clinical research protocol approved by regulatory authorities.
- Ensure that informed consent has been obtained using the version approved by the Research Ethics Committee (CEIm) and properly documented in the patient's medical records.
- Perform Source Data Verification (SDV), ensuring that data recorded in Case Report Forms (CRFs/eCRFs) matches source documents (medical records, laboratory reports, etc.), verifying accuracy, completeness, and traceability.
- Oversee safety reporting and the notification of adverse events, particularly Serious Adverse Events (SAEs), ensuring timely reporting according to regulatory requirements.
- Verify the receipt, storage, dispensing, accountability, and return or destruction of investigational medicinal products or study materials.
- Ensure that the Investigator Site File (ISF) and Trial Master File (TMF) are complete and up to date, including Ethics Committee approvals, regulatory approvals, delegation logs, team training records, CVs, certificates, and related documentation.
- Identify, document, and follow up protocol deviations and corrective actions.
- Provide support and training to site research teams and act as liaison with the sponsor.
- Apply risk-based monitoring strategies in accordance with the unit’s Standard Operating Procedures (SOPs).
Offered
- Permanent contract linked to the project. This position is initially funded by the Instituto de Salud Carlos III under grant reference PT23/00176 and co-funded by the European Union.
- Annual working schedule of 1,627.5 hours (37.5 hours per week).
- Salary according to ISCIII salary scales.
- Research Group: UICEC.
Documentation and deadline for submission
Interested parties should preferably deliver the documentation (1) in PDF, by e-mail to the Management of the Santa Creu i Sant Pau Hospital Research Institute Foundation, address ir_seleccio@santpau.cat , indicating the reference 2026/098:
(1) Application letter and updated Curriculum Vitae and signed Data Processing Authorization**
At the request of the Santa Creu i Sant Pau Hospital Research Institute Foundation, the candidates must present the documentation accrediting the merits mentioned in the curriculum vitae. Applications will be resolved within a maximum period of one month from the end of the deadline for submission of documentation. At the end of this period, without having been notified of an express resolution, the interested parties will be entitled to understand that their applications have been rejected. Santa Creu i Sant Pau Hospital Research Institute Foundation may declare this call for applications closed if, according to its criteria, the candidates does not meet the conditions that the Institution considers necessary to fill the position. The interpretation of the requirements and their enforceability to the candidates will be exclusive to the Santa Creu i Sant Pau Hospital Research Institute Foundation.
**It is essential to attach the duly signed data processing authorization (document attached at the end of the call) **
The deadline for submitting applications will end on July 3th , 2026, at 3:00 p.m.
Barcelona, Tel: 93 291 90 50, NIF: G-60136934,