JOB DESCRIPTION
We are looking to hire a Data Entry Specialist to join the Clinical Research Unit. The successful candidate will be responsible for supportingdata collection and entry processes for clinical trials in the field of medical oncology, ensuring data quality and regulatory compliance in cancer research studies.
HOW TO APPLY
Interested persons must attach to the application:
* Motivation letter explaining their interest in the position.
* Updated CV.
* Contact of 2-3 references.
Applications will be evaluated in accordance with the guiding principles and objectives of the supply systems, following the process described below:
1. Curricular evaluation: analysis of the curriculum vitae to assess aspects related to training, professional career and experience in positions related to the job position under selection.
2. Personal interview: once the résumé has been evaluated, the selected candidates will be called for a personal interview to verify and expand on the information detailed in the résumé and to evaluate aspects related to experience and professional skills.
Applications that do not meet the requirements, that are not included in the cases foreseen or that are not processed in accordance with the established procedure will not be considered in the selection process.
QUALIFICATIONS AND EXPERIENCIE
* Advanced Vocational Training (CFGS) in Healthcare Documentation and Administration.
* A university degree in Life Sciences will be an asset.
* Training in clinical trials and clinical research.
* Proficiency in English (spoken and written).
* Good command of IT tools and data management systems.
* Strong teamwork skills and ability to work under pressure.
Desirable:
* Previous experience in medical oncology clinical trials will be highly valued.
WHAT WE OFFER
* Indefinite contract (Contrato indefinido por actividades científico-técnicas 14/2011)
* Full time: 39h/week
* Immediate incorporation.
* Flexible payment (childminding vouchers + restaurant ticket).
* 23 days holiday and 5 days for personal matters.
* Training capsules by the company.
* Be part of an excellent multidisciplinary research centre with the HRS4R badge.
* Location on the Can Ruti Campus, a first-class translational research environment in the Barcelona area, in a very stimulating scientific environment. The IGTP offers a supportive, friendly and collaborative ecosystem to promote professional development and help you achieve your research goals.
FOR MORE INFORMATION
DEADLINE FOR APPLICATIONS
The call for applications will close on17th August, 2025
MAIN RESPONSIBILITIES
* Completion of Case Report Forms (CRFs) with accurate and up-to-date clinical data.
* Management and resolution of queries related to clinical trial data.
* Liaison with Sponsors and Contract Research Organizations (CROs) to ensure smooth communication and coordination.
* Preparation and support during monitoring visits, audits, and inspections, both internal and external.
* Participation in internal meetings and external information sessions related to clinical trials.
RESOLUCION
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