2026_121_STUDY COORDINATOR

IGTP Retreat; Badalona; Presencial; EUR 29.000 - 36.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Childcare vouchers

23 days holiday & 5 personal days

Training capsules

Descripción de la vacante

IGTP needs to incorporate a clinical trial coordinator in the clinical research unit of ICO to carry out oncology clinical trials.

The role involves designing data collection documentation, supervising sample collection, preparing materials, scheduling treatments, and ensuring trial materials are reviewed and controlled. Immediate incorporation and a permanent contract are offered.

Formación

• 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.
• Nice to have: oncology clinical trials experience (hematologic and solid tumours).

Responsabilidades

• 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.

Conocimientos

Teamwork

Work under pressure

Communication

Educación

Degree in life sciences

Training in clinical trials and clinical research

Experience as study coordinator

Herramientas

MS Office

Descripción del empleo

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

DEADLINE FOR APPLICATIONS

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