26-126_SS_VN Study Coordinator for Cancer Clinical Trials (España)

26-126_SS_VN Study Coordinator for Cancer Clinical Trials (España)

26 ago
|
Institut D'Investigació Biomédica De Bellvitge (Idibell)
|
España

26 ago

Institut D'Investigació Biomédica De Bellvitge (Idibell)

España

Organisation/Company Institut d'Investigacio Biomedica de Bellvitge (IDIBELL) Department RRHH Research Field Biological sciences Other Researcher Profile Other Profession Positions Bachelor Positions Application Deadline 7 Oct 2026 - 23:59 (Europe/Madrid) Country Spain Type of Contract Permanent Job Status Full-time Hours Per Week 40 Offer Starting Date 21 Sep 2026 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Reference Number 26-126_SS_VN Is the Job related to staff position within a Research Infrastructure? No

Lea atentamente toda la información sobre esta oportunidad y luego utilice el botón de solicitud de abajo para enviar su CV y su candidatura.
Offer Description
Our institute

IDIBELL is a research center that integrates the biomedical research of the Bellvitge University Hospital (HUB), the Catalan Institute of Oncology (ICO), and the University of Barcelona in the Bellvitge Campus (UB), and the Viladecans Hospital (HV). The research focuses of IDIBELL are cancer, neuroscience, translational medicine and regenerative medicine. Research, innovation and society are the pivots on which researchers work every day in order to improve the quality of life of citizens. IDIBELL is located in L’Hospitalet de Llobregat, south of Barcelona. It is a member of the Campus of International Excellence of the University of Barcelona (HUBc) and Research Centers of Catalonia (CERCA). In 2009, it became one of the first five Spanish research centers accredited as a health research institute by the Health Institute Carlos III. In 2015, the European Commission recognized IDIBELL with the 'HR Excellence in Research' award, which identifies IDIBELL as a provider and supporter of a stimulating research work environment.

About the research group/unit

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 trial.

About the role

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- Coordination of Oncology Clinical Trials (Haematology Diseases ) into Clinical Research unit for advanced phase trials.

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- Performance and application of coordinated procedures between the different clinical services involved in the inclusion,



treatment and follow-up of patient’s participation.

- Support to Investigators and electronic tools implementation.

- Management of human tissues between different external referring sites.

- Record of transactions in sponsor’s systems (IWR). Record of trial and patient’s information into clinical and research applications.

- Administrative procedures during the study

- SAE completion

- Case Report Form training, completion and correction. Queries resolution.

- Communication with Sponsors and CROs.

- Preparation and attention to monitoring visits, audits and inspections, internal and external information meetings.

Job requirements

Professional experience

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- At minimum of 6 months of experience in oncology or hematology cancer clinical trials ( as coordinator or data entry)

- Coordination or data entry in phase I, II and III cancer trials

Education and training

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- Education In clinical trials and clinical research

- Education in Good Clinical Practices

Technical skills

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- Office (Outlook, Excel, Word), internet, patients files

- 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

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- Good command of the English language

We will value, but not required

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- Experience as Clinical trials Monitor

- Familiarity with SAP Argos Electronic Medical Record syste

- Previous experience in data management of oncology studies

- Previous experience in clinical trials (other than cancer)

What do we offer

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- No. of positions: 1

- Estimated start date: 21/09/2026

- Contract duration: Permanent by project

- Estimated annual gross salary: 33.804,17€

- 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. Please express yourself freely, safely and non-binarily, if that's the case.

Data protection notice

In compliance with the obligations established in the General Regulation of Data Protection (RGPD), which is the Regulation (EU) 2016/679 of the Parliament and of the Council, of April 27, 2016, and the Organic Law 3/2018, of December 5, Protection of Personal Data and guarantee of digital rights, it is reported that the Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), CIF G , with address Av. Granvia de l'Hospitalet, 199-203, 08908, L'Hospitalet de Llobregat, will process your personal data, as the controller, to apply for the position, maintain communication concerning the status of the candidature, to access the delivered CV; to compare that your data is in accordance with the offers announced by IDIBELL and to verify, where appropriate, that the information provided is accurate. You can find more information in our Privacy Policy at " " , request more information about the data processing carried out and exercise your rights of access, rectification, deletion, opposition, portability, limitation of processing by sending a request at email: . If you consider that you have not obtained satisfaction in exercising your rights, you may submit a claim to Catalan Data Protection Authority.

Our institute

IDIBELL is a research center that integrates the biomedical research of the Bellvitge University Hospital (HUB), the Catalan Institute of Oncology (ICO), and the University of Barcelona in the Bellvitge Campus (UB), and the Viladecans Hospital (HV). The research focuses of IDIBELL are cancer, neuroscience, translational medicine and regenerative medicine. Research, innovation and society are the pivots on which researchers work every day in order to improve the quality of life of citizens. xqbhyrx

IDIBELL is committed to the principles of the Code of Conduct for the Recruitment of Researchers of the European Commission and the implementation of open, transparent and merit-based recruitment (OTMR).

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📌 26-126_SS_VN Study Coordinator for Cancer Clinical Trials (España)
🏢 Institut D'Investigació Biomédica De Bellvitge (Idibell)
📍 España

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