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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 €
- Versátil 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. xugodme The IGTP offers a supportive, friendly and collaborative ecosystem to promote professional development and help you achieve your research goals.

FOR MORE INFORMATION FOR APPLICATIONS The call for applications will close on September 21st, 2026

📌 2026_121_STUDY COORDINATOR (Municipio de Badalona)
🏢 IGTP Retreat
📍 Municipio de Badalona