Responsible, organised and decisive person with extensive experience in coordinating clinical trials, preferably with work experience in research centres or similar.

Previous accredited experience in the following functions is required:

-Completing the database of the national study in inflammatory disease with the data provided in the history by all participating centre investigators.

- Sending samples to central laboratories, in clinical trials conducted in the inflammatory unit.

- Study coordinator, in clinical trials in the Inflammatory Bowel Disease Unit: completing the data collection notebooks, monitoring the appropriate follow-up of patient visits supervised by the principal investigator of the project in each case.

- Coordination of studies carried out in the Unit: creation of CRD, protocols, bureaucratic procedures for starting studies, patient monitoring.

- Coordination with the Hospital Pharmacy Service for the medication dispensed in clinical trials.

Gross annual salary: 27.572,31.-€. 

Holidays: 22 working days and 6 days for private matters.

Working hours: 37.5 hours per week.

Depending on the candidate's experience, training and skills

A personal interview will be held.

The candidate will be evaluated by the internal Scientific Committee of the institution.

Candidates wishing to register should indicate in the reference "Eurassex Study Coordinator (MDMA)