ppICO-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 /ph3About the role /h3ulliSupervision and distribution of tasks and charges of the different study coordinators, data entries and regulatory personnel ( allocation and follow-up). /liliSupervision that personnel executes standard operating procedures according to the quality plan (daily operations, non-conformities, support for trials audits and inspections). /liliPersonnel management (permissions and holidays, work from home, and location managements and sick leave support). /liliPersonnel meetings with principal investigators and writing minutes. /liliCoordinated work with other areas of UIC (economic management, etc). /li /ulh3Job requirements /h3pProfessional experience /pulliAt minimum of 3 years as study coordinator. /liliExperience with clinical trials audits or inspections as study coordinator. /liliTraining or experience in medical oncology /li /ulpEducation and training /pulliEducation In clinical trials and clinical research. , /liliEducation in Good Clinical Practices /li /ulh3Technical soft skills /h3ulliOffice (Outlook, Excel, Word), internet, patients files. /liliPersonnel management and leadership of labor relations. /liliTo organize, order, and perform different activities with knowledge of their influence on the final outcome of a process.



/liliUnderstand the points of view of other people, give help. /liliAbility to work under pressure. /li /ulh3Languages /h3ulliGood command of the English language /li /ulh3We will value, but not required /h3ulliExperience as Clinical trials Monitor. /liliFamiliarity with SAP Argos Electronic Medical Record system. /liliPrevious experience in data management of oncology studies. /liliPrevious experience in clinical trials (other than cancer). /li /ulh3What do we offer /h3ullibNo. of positions: /b 1 /lilibEstimated start date: /b 14/09/2026 /lilibContract duration: /b Permanent linked to a project /lilibEstimated annual gross salary: /b salary is commensurate with qualifications and consistent with our pay ranges. /liliYou will be part of a bmulticultural team. /b We have a fun loving and friendly international work environment. /lilibFlexible working schedule /b - We know you have a life outside of work and we will work with you to make sure it's kept that way. /liliPossibility to work some days in remote -bTeleworking /b /lilib26 working days of holiday /b per year /lilibSystem of accumulated hours /b for employees, from 88 to 104 hours depending on the year (11 to 13 working days), to attend to personal matters /liliPbaid leave package. /b /liliBenefits of constant training are offered /lilibWe offer and promote diverse and inclusive conditions /b. 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. Please express yourself freely, safely and non-binarily, if that's the case. /li /ulpbDeadline: /b Please submit your application by15 August 2026 /p /p #J-18808-Ljbffr

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