2026_121_STUDY COORDINATOR

Full Job Description

IGTP needs to incorporate a clinical trial coordinator in the clinical research unit of the Catalan Oncology Institute (ICO) to carry out tasks in oncology clinical trials.

Main Responsibilities

• Design the specific documentation for data collection related to nursing procedures and activities
• Supervise the collection of samples and the performance of specific procedures for trial patients
• Prepare materials for sample collection
• Supervise and adjust treatment scheduling
• Review and control trial materials

Qualifications And Experiencie

• Degree in life sciences.
• Training in clinical trials and clinical research (Master or similar).
• At least six months of experience as study coordinator.
• Accredit a good level of angles and knowledge of computer tools.
• Ability to work in teams and under pressure.

It will be valued positively:

• Previous experience in clinical trials of oncology, including both hematologic and solid tumours.

What we offer

• Permanent contract under the Science Law 14/2011.
• Full-time working schedule.
• Immediate incorporation.
• Gross remuneration of 32.522,76 €
• Flexible payment (childminding vouchers).
• 23 days holiday and 5 days for personal matters.
• Training capsules by the company.
• Be part of an excellent multidisciplinary research centre with the HRS4R badge.
• Location on the Can Ruti Campus, a first-class translational research environment in the Barcelona area, in a very stimulating scientific environment. The IGTP offers a supportive, friendly and collaborative ecosystem to promote professional development and help you achieve your research goals.

For More Information

https://ico.gencat.cat/es/inici

How to apply

Interested persons must attach to the application:

• Motivation letter explaining their interest in the position.
• Updated CV.
• Contact of 2-3 references.

Applications will be evaluated in accordance with the guiding principles and objectives of the supply systems, following the process described below:

• Curricular evaluation: analysis of the curriculum vitae to assess aspects related to training, professional career and experience in positions related to the job position under selection.
• Personal interview: once the résumé has been evaluated, the selected candidates will be called for a personal interview to verify and expand on the information detailed in the résumé and to evaluate aspects related to experience and professional skills.

Applications that do not meet the requirements, that are not included in the cases foreseen or that are not processed in accordance with the established procedure will not be considered in the selection process.

Deadline For Applications

The call for applications will close on September 21st, 2026

• Degree in life sciences.
• Training in clinical trials and clinical research (Master or similar).
• At least six months of experience as study coordinator.
• Accredit a good level of angles and knowledge of computer tools.
• Ability to work in teams and under pressure.

It will be valued positively:

• Previous experience in clinical trials of oncology, including both hematologic and solid tumours.

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