12 ago
|
BELLVITGE BIOMEDICAL RESEARCH INSTITUTE (IDIBELL)
|
España
12 ago
BELLVITGE BIOMEDICAL RESEARCH INSTITUTE (IDIBELL)
España
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
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 requirements
Professional 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 Ele
📌 Area Coordinator (España)
🏢 BELLVITGE BIOMEDICAL RESEARCH INSTITUTE (IDIBELL)
📍 España