JOB DESCRIPTIONIGTP 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 materialsQUALIFICATIONS 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 €- Adaptable 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 INFORMATIONhttps://ico.Gencat.Cat/es/iniciDEADLINE FOR APPLICATIONSThe call for applications will close on September 21st, 2026#J-18808-Ljbffr

📌 2026_121_study Coordinator (Badalona)
🏢 IGTP Retreat
📍 Badalona