Closed

T4 PT ISCIII 23

Barcelona Ref. 2026/093

Deadline: 29 June 2026, 3:00 pm

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

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