ICO-L'Hospitalet is a reference hospital for the clinical research in cancer. Their two units (UIC and UFF1) have been participating in 602 clinical trials with active recruitment or with current activities during 2025 and 695 patients decided to participate in them. Many of these trials are testing the most promising therapies in cancer and investigators involved in them are specialized and up-to-date with the latest advances in new treatments.

UIC and UFF1 units have the best professionals who carry out the most demanding clinical trials

Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada.

About the role

- Supervision and distribution of tasks and charges of the different study coordinators, data entries and regulatory personnel ( allocation and follow-up).
- Supervision that personnel executes standard operating procedures according to the quality plan (daily operations, non-conformities, support for trials audits and inspections).
- Personnel management (permissions and holidays, work from home, and location managements and sick leave support).
- Personnel meetings with principal investigators and writing minutes.
- Coordinated work with other areas of UIC (economic management, etc).

Job requirementsProfessional experience
- At minimum of 3 years as study coordinator.
- Experience with clinical trials audits or inspections as study coordinator.
- Training or experience in medical oncology

Education and training
- Education In clinical trials and clinical research. ,
- Education in Good Clinical Practices

Technical & soft skills
- Office (Outlook, Excel, Word), internet, patients files.
- Personnel management and leadership of labor relations.




- To organize, order, and perform different activities with knowledge of their influence on the final outcome of a process.
- Understand the points of view of other people, give help.
- Ability to work under pressure.

Languages
- Good command of the English language

We will value, but not required
- Experience as Clinical trials Monitor.
- Familiarity with SAP Argos Electronic Medical Record system.
- Previous experience in data management of oncology studies.
- Previous experience in clinical trials (other than cancer).

What do we offer
- No. of positions: 1
- Estimated start date: 14/09/2026
- Contract duration: Permanent linked to a project
- Estimated annual gross salary: salary is commensurate with qualifications and consistent with our pay ranges.
- You will be part of a multicultural team. We have a fun loving and friendly international work environment.
- Adaptable working schedule - We know you have a life outside of work and we will work with you to make sure it's kept that way.
- Possibility to work some days in remote -Teleworking
- 26 working days of holiday per year
- System of accumulated hours for employees, from 88 to 104 hours depending on the year (11 to 13 working days), to attend to personal matters
- Paid leave package.
- Benefits of constant training are offered
- We offer and promote diverse and inclusive conditions. Applicants are made free from any discrimination. Specifically IDIBELL works to improve gender equality in all areas with the aim of achieving gender balance, but maintaining the most scrupulous respect to any choice at the level of gender identity. xqbhyrx Please express yourself freely, safely and non-binarily, if that's the case.

Deadline: Please submit your application by15 August 2026

📌 Area Coordinator – Medical Oncology Clinical Trials (L'Hospitalet de Llobregat)
🏢 BELLVITGE BIOMEDICAL RESEARCH INSTITUTE (IDIBELL)
📍 L'Hospitalet de Llobregat