Select which cookies you accept
When you visit this website, it may store or retrieve information on your browser, mostly in the form of cookies. This information might be about you, your preferences or your device and is mostly used to make the website work as you expect it to. The information does not usually directly identify you, but it can give you a more personalized web experience.
Because we respect your right to privacy, you can choose not to allow some types of cookies. Below is a list of different categories of cookies that may be set and that you can freely change. However, blocking some types of cookies may impact your experience of the site and the services we are able to offer.
These cookies are required and must be accepted to use this site.
These cookies collect data about how visitors use this website.
These cookies allow the website to remember choices you make and provide enhanced, more personal features.
These cookies are used to deliver adverts more relevant to you and your interests.
IDIBELL is looking for a Data Entry for Cancer Clinical Trials
About the research group
ICO-L’Hospitalet is a reference hospital for the clinical research in cancer. Their two units (UIC and UFF1) have been participating in 545 clinical trials with active recruitment or with current activities during 2021 and 676 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 they are the best professionals who carry out the most demanding clinical trials
About the role
Integration into Clinical Research Unit and Functional Phase I Unit team and Investigator’s teams as data entry.
Case Report Form training, completion and correction.
Support to Investigators and electronic tools implementation.
Record of trial and patient’s information into clinical and research applications.
Communication with Sponsors and CROs.
Set-up and attention to monitoring visits, audits and inspections.
Practical management of cancer clinical trials
Education and training
University degree in life Science or Senior Technician in Health Documentation and Administration or similar studies regarding to health sciences.
Education in clinical trials
Certifyed training in Good Clinical Practices.
Office (Outlook, word, excel)
Clinical trials case report forms
To organize, order and perform different activities with knowledge of their influence on the final outcome of a process. Understand the points ov view of other peole, give help. Ability to work under pressure.
Good command of the English language
Perfect command of Spanish and Catalan language
We will value, but not required
Previous experience in data management or coordination of cancer clinical trials
Familiarity with SAP ARGOS electronic medical record system
What do we offer
Nº of positions: 1
Start date: may 2022
Contract duration: Permanent linked to project
Estimated annual gross salary: it 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.
Flexible 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.
Benefits of constant training are offered.
We offer and promote diverse and inclusive conditions. Applicants are made free from any discrimination.
Pre-selection: The pre-selection process will consist on an eligibility check based on qualifications and expertise reflected on the candidate's CV.
Interview: Best positioned, pre-selected candidates may be called to arrange an interview. Candidates will be interviewed by the hiring manager and an ad hoc selection panel.
Formal offer letter: Once identified, the People Management Unit will send a job offer to the successful candidate indicating start date, salary, working conditions, and any additional relevant details.
Deadline: Please submit your application by 11 May 2022
Data protection notice
IDIBELL ensures that applicants’ personal data are processed as required by the EU General Data Protection Regulation (GDPR) and Spanish Law 3/2018 on Data Protection. Personal data is processed solely for the purpose of the selection procedure.
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 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).
Bellvitge Biomedical Research Institute is focused in cancer, neuroscience, translational medicine and regenerative medicine. Research, innovation and society are the axes on which researchers work every day with the goal of improving the quality of life of citizens.
Our mission is to carry out research of excellence that integrates knowledge and innovation in health, contributing to the improvement of people's quality of life.
Our vision of future is to become a European reference in health sciences, rooted in our local environment and contributing to its growth by attracting and retaining research talent in health sciences.
In order to fullfil both, our values are: integrity, confidence, transparency, aspiration, passion and commitment.
Data Entry for Cancer Clinical Trials
Loading application form
Already working at IDIBELL?
Let’s recruit together and find your next colleague.