The Data Management Center at the European Foundation for the Study of Chronic Liver Failure (EF CLIF) is expanding its scope to conduct large-scale observational studies and clinical trials of increasing complexity.
We are looking for a biostatistician to provide statistical expertise in the design of statistical analysis plans (SAPs) for research projects and clinical trials, referring to senior statistical experts where necessary. You will manage your own projects within your working schedule and apply a range of statistical methods to solve complex problems as part of a multidisciplinary team.
The candidate's responsibilities include :
The successful candidate will join the Data Management Center, which coordinates all activities related to the development of clinical platforms, data cleansing processes, and biological sample management. The team is currently constituted by 4 members including bioinformaticians, statisticians, data managers, and the CTIO.
Throughout the data lifecycle, from collection and preservation to analysis and dissemination, the Data Management Center operates in accordance with the FAIR principles – making data findable, accessible, interoperable and reusable, applying the highest standards in clinical research and in compliance with the General Data Protection Regulation (GDPR).
The Data Management Center is based in the EF CLIF Headquarters in Barcelona, Spain, and serves as a resource for our members and collaborators in tertiary care university hospitals across the world, enabling access to relevant clinical and laboratory data, and specimens through a secure environment.
The Data Management Center plays an important role in the design and development of the databases and protocols for all EF CLIF sponsored studies, ensures good research data management, assists regional coordinator with protocol implementation, tracks specimen information, delivers remote training across study sites, and contributes to data analysis and manuscript preparation.
Moreover, the Data Management Center provides support in the study design and work planning of research project proposals, as well as bioinformatics and statistical expert consultation.
Requisites
Professional experience :
Education and training :
3 years practical experience in applying statistics in clinical trials
Technical skills :
Competences :
J-18808-Ljbffr
The • barcelona, España